#Uploaded_variation	Location	Allele	Gene	Feature	Feature_type	Consequence	cDNA_position	CDS_position	Protein_position	Amino_acids	Codons	Existing_variation	Extra
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1173	1031	344	L/P	cTg/cCg	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1297	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1167	1031	344	L/P	cTg/cCg	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1224	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4551;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	973	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	913	635	212	L/P	cTg/cCg	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3848;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4438;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2857;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1046	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3539;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3576;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4484;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1281	914	305	L/P	cTg/cCg	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1224	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	973	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1046	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	913	554	185	L/P	cTg/cCg	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1167	914	305	L/P	cTg/cCg	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1221	914	305	L/P	cTg/cCg	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1297	-	-	-	-	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12375	17:7670678-7670678	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1174	914	305	L/P	cTg/cCg	rs121912662,CM961377,COSV52687285,COSV53045945,COSV53068361	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1167	1025	342	R/P	cGa/cCa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1291	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1161	1025	342	R/P	cGa/cCa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1218	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4545;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	967	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	907	629	210	R/P	cGa/cCa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3842;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4432;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2851;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1040	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3533;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3570;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4478;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1275	908	303	R/P	cGa/cCa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1218	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	967	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1040	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	907	548	183	R/P	cGa/cCa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1161	908	303	R/P	cGa/cCa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1215	908	303	R/P	cGa/cCa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1291	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
215996	17:7670684-7670684	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1168	908	303	R/P	cGa/cCa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1152	1010	337	R/L	cGc/cTc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1276	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1146	1010	337	R/L	cGc/cTc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1203	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4530;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	952	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	892	614	205	R/L	cGc/cTc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3827;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4417;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2836;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1025	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3518;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4463;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1260	893	298	R/L	cGc/cTc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1203	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	952	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1025	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	892	533	178	R/L	cGc/cTc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1146	893	298	R/L	cGc/cTc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1200	893	298	R/L	cGc/cTc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1276	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142828	17:7670699-7670699	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1153	893	298	R/L	cGc/cTc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1152	1010	337	R/P	cGc/cCc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1276	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1146	1010	337	R/P	cGc/cCc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1203	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4530;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	952	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	892	614	205	R/P	cGc/cCc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3827;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4417;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2836;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1025	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3518;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4463;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1260	893	298	R/P	cGc/cCc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1203	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	952	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1025	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	892	533	178	R/P	cGc/cCc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1146	893	298	R/P	cGc/cCc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1200	893	298	R/P	cGc/cCc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1276	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
177879	17:7670699-7670699	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1153	893	298	R/P	cGc/cCc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1152	1010	337	R/H	cGc/cAc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1276	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1146	1010	337	R/H	cGc/cAc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1203	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4530;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	952	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	892	614	205	R/H	cGc/cAc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3827;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4417;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2836;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1025	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3518;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4463;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1260	893	298	R/H	cGc/cAc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1203	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	952	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1025	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	892	533	178	R/H	cGc/cAc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1146	893	298	R/H	cGc/cAc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1200	893	298	R/H	cGc/cAc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1276	-	-	-	-	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12379	17:7670699-7670699	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1153	893	298	R/H	cGc/cAc	rs121912664,CM012663,CM104660,COSV52665150,COSV52691988,COSV52828545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1151	1009	337	R/C	Cgc/Tgc	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1275	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1145	1009	337	R/C	Cgc/Tgc	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1202	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4529;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	951	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	891	613	205	R/C	Cgc/Tgc	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3826;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4416;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2835;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1024	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3517;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3554;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4462;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1259	892	298	R/C	Cgc/Tgc	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1202	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	951	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1024	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	891	532	178	R/C	Cgc/Tgc	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1145	892	298	R/C	Cgc/Tgc	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1199	892	298	R/C	Cgc/Tgc	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1275	-	-	-	-	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
142536	17:7670700-7670700	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1152	892	298	R/C	Cgc/Tgc	rs587782529,CM981929,COSV52669243,COSV52718762,COSV52810068,COSV52816817	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1029	887	296	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	887	887	296	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1020	887	296	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1023	887	296	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1020	887	296	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1496;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	769	491	164	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	769	491	164	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=793;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1383;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	623	491	164	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	769	491	164	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=484;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=521;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=146;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1429;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1137	770	257	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1020	770	257	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	769	410	137	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	769	410	137	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	769	410	137	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1023	770	257	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1077	770	257	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1020	770	257	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1030	770	257	H/R	cAc/cGc	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
100816	17:7673733-7673733	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs483352696,COSV52661430,COSV53423770,COSV53715451	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	998	856	286	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	856	856	286	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	989	856	286	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	992	856	286	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	989	856	286	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1465;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	738	460	154	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	738	460	154	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=762;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1352;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	592	460	154	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	738	460	154	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=453;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=490;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=177;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1398;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1106	739	247	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	989	739	247	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	738	379	127	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	738	379	127	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	738	379	127	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	992	739	247	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1046	739	247	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	989	739	247	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	999	739	247	E/K	Gaa/Aaa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
183752	17:7673764-7673764	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	996	854	285	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	854	854	285	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	987	854	285	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	990	854	285	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	987	854	285	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1463;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	736	458	153	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	736	458	153	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=760;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1350;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	590	458	153	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	736	458	153	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=451;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=488;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=179;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1396;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1104	737	246	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	987	737	246	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	736	377	126	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	736	377	126	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	736	377	126	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	990	737	246	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1044	737	246	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	987	737	246	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	997	737	246	E/V	gAg/gTg	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12384	17:7673766-7673766	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs121912667,CM083790,COSV52676438,COSV53038615,COSV53625652	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	986	844	282	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	844	844	282	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	977	844	282	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	980	844	282	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	977	844	282	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1453;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	726	448	150	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	726	448	150	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=750;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1340;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	580	448	150	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	726	448	150	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=441;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=478;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=189;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1386;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1094	727	243	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	977	727	243	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	726	367	123	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	726	367	123	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	726	367	123	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	980	727	243	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1034	727	243	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	977	727	243	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	987	727	243	R/W	Cgg/Tgg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12364	17:7673776-7673776	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	986	844	282	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	844	844	282	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	977	844	282	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	980	844	282	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	977	844	282	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1453;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	726	448	150	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	726	448	150	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=750;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1340;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	580	448	150	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	726	448	150	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=441;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=478;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=189;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1386;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1094	727	243	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	977	727	243	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	726	367	123	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	726	367	123	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	726	367	123	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	980	727	243	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1034	727	243	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	977	727	243	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	987	727	243	R/G	Cgg/Ggg	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
140821	17:7673776-7673776	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs28934574,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	984	842	281	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	842	842	281	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	975	842	281	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	978	842	281	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	975	842	281	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1451;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	724	446	149	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	724	446	149	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1338;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	578	446	149	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	724	446	149	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=439;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=476;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=191;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1384;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1092	725	242	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	975	725	242	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	724	365	122	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	724	365	122	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	724	365	122	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	978	725	242	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1032	725	242	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	975	725	242	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	985	725	242	D/V	gAc/gTc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
182968	17:7673778-7673778	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	984	842	281	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	842	842	281	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	975	842	281	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	978	842	281	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	975	842	281	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1451;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	724	446	149	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	724	446	149	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1338;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	578	446	149	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	724	446	149	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=439;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=476;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=191;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1384;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1092	725	242	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	975	725	242	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	724	365	122	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	724	365	122	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	724	365	122	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	978	725	242	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1032	725	242	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	975	725	242	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	985	725	242	D/G	gAc/gGc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
141141	17:7673778-7673778	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	981	839	280	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	839	839	280	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	972	839	280	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	975	839	280	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	972	839	280	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1448;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	721	443	148	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	721	443	148	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=745;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1335;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	575	443	148	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	721	443	148	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=436;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=473;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=194;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1381;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1089	722	241	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	972	722	241	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	721	362	121	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	721	362	121	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	721	362	121	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	975	722	241	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1029	722	241	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	972	722	241	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	982	722	241	R/T	aGa/aCa	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12368	17:7673781-7673781	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs121912660,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	969	827	276	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	827	827	276	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	960	827	276	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	963	827	276	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	960	827	276	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1436;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	709	431	144	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	709	431	144	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=733;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1323;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	563	431	144	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	709	431	144	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=424;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=461;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=206;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1369;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1077	710	237	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	960	710	237	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	709	350	117	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	709	350	117	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	709	350	117	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	963	710	237	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1017	710	237	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	960	710	237	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	970	710	237	A/G	gCc/gGc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185319	17:7673793-7673793	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	969	827	276	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	827	827	276	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	960	827	276	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	963	827	276	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	960	827	276	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1436;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	709	431	144	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	709	431	144	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=733;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1323;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	563	431	144	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	709	431	144	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=424;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=461;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=206;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1369;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1077	710	237	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	960	710	237	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	709	350	117	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	709	350	117	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	709	350	117	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	963	710	237	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1017	710	237	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	960	710	237	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	970	710	237	A/D	gCc/gAc	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
232683	17:7673793-7673793	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs786202082,CD098502,COSV52704969,COSV52749634,COSV52761908,COSV52834111	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	966	824	275	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	824	824	275	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	957	824	275	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	960	824	275	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	957	824	275	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1433;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	706	428	143	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	706	428	143	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=730;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1320;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	560	428	143	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	706	428	143	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=421;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=458;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=209;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1366;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1074	707	236	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	957	707	236	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	706	347	116	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	706	347	116	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	706	347	116	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	960	707	236	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1014	707	236	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	957	707	236	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	967	707	236	C/Y	tGt/tAt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
215997	17:7673796-7673796	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	960	818	273	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	818	818	273	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	951	818	273	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	954	818	273	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	951	818	273	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1427;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	700	422	141	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	700	422	141	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=724;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1314;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	554	422	141	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	700	422	141	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=415;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=452;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=215;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1360;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1068	701	234	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	951	701	234	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	700	341	114	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	700	341	114	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	700	341	114	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	954	701	234	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1008	701	234	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	951	701	234	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
231060	17:7673802-7673802	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	961	701	234	R/P	cGt/cCt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	960	818	273	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	818	818	273	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	951	818	273	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	954	818	273	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	951	818	273	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1427;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	700	422	141	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	700	422	141	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=724;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1314;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	554	422	141	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	700	422	141	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=415;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=452;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=215;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1360;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1068	701	234	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	951	701	234	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	700	341	114	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	700	341	114	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	700	341	114	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	954	701	234	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1008	701	234	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	951	701	234	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12366	17:7673802-7673802	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	961	701	234	R/H	cGt/cAt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	959	817	273	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	817	817	273	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	950	817	273	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	953	817	273	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	950	817	273	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1426;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	699	421	141	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	699	421	141	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=723;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1313;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	553	421	141	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	699	421	141	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=414;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=451;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=216;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1359;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1067	700	234	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	950	700	234	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	699	340	114	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	699	340	114	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	699	340	114	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	953	700	234	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1007	700	234	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	950	700	234	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
43594	17:7673803-7673803	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	960	700	234	R/C	Cgt/Tgt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	957	815	272	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	815	815	272	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	948	815	272	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	951	815	272	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	948	815	272	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1424;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	697	419	140	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	697	419	140	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=721;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1311;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	551	419	140	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	697	419	140	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=412;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=449;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=218;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1357;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1065	698	233	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	948	698	233	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	697	338	113	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	697	338	113	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	697	338	113	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	951	698	233	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1005	698	233	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	948	698	233	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233323	17:7673805-7673805	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	958	698	233	V/G	gTg/gGg	rs876660333,CM942122,COSV52701102,COSV52773741,COSV52787833,COSV53259929	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	956	814	272	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	814	814	272	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	947	814	272	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	950	814	272	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	947	814	272	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1423;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	696	418	140	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	696	418	140	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1310;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	550	418	140	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	696	418	140	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=411;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=448;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=219;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1356;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1064	697	233	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	947	697	233	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	696	337	113	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	696	337	113	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	696	337	113	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	950	697	233	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1004	697	233	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	947	697	233	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
185814	17:7673806-7673806	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	957	697	233	V/M	Gtg/Atg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	941	799	267	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	799	799	267	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	932	799	267	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	935	799	267	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	932	799	267	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1408;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	681	403	135	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	681	403	135	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=705;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1295;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	535	403	135	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	681	403	135	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=396;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=433;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=234;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1341;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1049	682	228	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	932	682	228	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	681	322	108	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	681	322	108	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	681	322	108	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	935	682	228	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	989	682	228	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	932	682	228	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141764	17:7673821-7673821	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	942	682	228	R/W	Cgg/Tgg	rs55832599,CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	936	794	265	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	794	794	265	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	927	794	265	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	930	794	265	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	927	794	265	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1403;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	676	398	133	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	676	398	133	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=700;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1290;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	530	398	133	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	676	398	133	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=391;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=428;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=239;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1336;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1044	677	226	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	927	677	226	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	676	317	106	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	676	317	106	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	676	317	106	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	930	677	226	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	984	677	226	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	927	677	226	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
245777	17:7673826-7673826	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	937	677	226	L/P	cTg/cCg	rs879253942,CD004355,CM971505,COSV52706540,COSV52732531,COSV53696163	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	914	772	258	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	772	772	258	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	772	772	258	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	905	772	258	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	908	772	258	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	905	772	258	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1038;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	654	376	126	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	654	376	126	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=335;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=925;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	508	376	126	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	654	376	126	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=26;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=63;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1022	655	219	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	905	655	219	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	654	295	99	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	654	295	99	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	654	295	99	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	908	655	219	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	962	655	219	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	905	655	219	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12348	17:7674191-7674191	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	915	655	219	E/K	Gaa/Aaa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	894	752	251	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	752	752	251	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	752	752	251	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	885	752	251	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	888	752	251	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	885	752	251	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1018;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	634	356	119	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	634	356	119	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=315;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	488	356	119	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	634	356	119	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=43;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=624;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=951;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1002	635	212	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	885	635	212	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	634	275	92	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	634	275	92	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	634	275	92	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	888	635	212	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	942	635	212	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	885	635	212	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182967	17:7674211-7674211	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	895	635	212	I/S	aTc/aGc	rs730882027,COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	893	751	251	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	751	751	251	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	751	751	251	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	884	751	251	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	887	751	251	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	884	751	251	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1017;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	633	355	119	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	633	355	119	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=314;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	487	355	119	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	633	355	119	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=42;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=625;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=950;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1001	634	212	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	884	634	212	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	633	274	92	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	633	274	92	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	633	274	92	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	887	634	212	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	941	634	212	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	884	634	212	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
182937	17:7674212-7674212	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	894	634	212	I/L	Atc/Ctc	rs730882007,CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	887	745	249	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	745	745	249	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	745	745	249	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	878	745	249	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	881	745	249	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	878	745	249	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1011;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	627	349	117	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	627	349	117	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=308;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=898;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	481	349	117	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	627	349	117	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000514944.5	Transcript	incomplete_terminal_codon_variant,coding_sequence_variant	545	466	156	X	Ag/Tg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=36;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=944;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	995	628	210	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	878	628	210	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	627	268	90	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	627	268	90	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	627	268	90	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	881	628	210	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	935	628	210	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	878	628	210	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
141881	17:7674218-7674218	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	888	628	210	R/W	Agg/Tgg	rs587782082,COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	885	743	248	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	743	743	248	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	743	743	248	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	876	743	248	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	879	743	248	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	876	743	248	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1009;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	625	347	116	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	625	347	116	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=306;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=896;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	479	347	116	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	625	347	116	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	543	464	155	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=34;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=942;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	993	626	209	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	876	626	209	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	625	266	89	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	625	266	89	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	625	266	89	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	879	626	209	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	933	626	209	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	876	626	209	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
230253	17:7674220-7674220	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	886	626	209	R/L	cGg/cTg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	885	743	248	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	743	743	248	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	743	743	248	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	876	743	248	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	879	743	248	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	876	743	248	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1009;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	625	347	116	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	625	347	116	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=306;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=896;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	479	347	116	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	625	347	116	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	543	464	155	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=34;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=942;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	993	626	209	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	876	626	209	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	625	266	89	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	625	266	89	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	625	266	89	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	879	626	209	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	933	626	209	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	876	626	209	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237954	17:7674220-7674220	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	886	626	209	R/P	cGg/cCg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	885	743	248	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	743	743	248	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	743	743	248	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	876	743	248	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	879	743	248	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	876	743	248	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1009;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	625	347	116	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	625	347	116	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=306;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=896;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	479	347	116	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	625	347	116	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	543	464	155	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=34;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=942;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	993	626	209	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	876	626	209	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	625	266	89	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	625	266	89	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	625	266	89	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	879	626	209	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	933	626	209	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	876	626	209	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12356	17:7674220-7674220	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	886	626	209	R/Q	cGg/cAg	rs11540652,CM920675,COSV52661091,COSV52661580,COSV52675468,COSV52802300	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	884	742	248	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	742	742	248	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	742	742	248	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	875	742	248	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	878	742	248	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	875	742	248	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1008;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	624	346	116	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	624	346	116	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=305;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	478	346	116	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	624	346	116	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	542	463	155	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=33;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=634;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=941;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	992	625	209	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	875	625	209	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	624	265	89	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	624	265	89	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	624	265	89	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	878	625	209	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	932	625	209	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	875	625	209	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12347	17:7674221-7674221	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	885	625	209	R/W	Cgg/Tgg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	878	736	246	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	736	736	246	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	736	736	246	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	869	736	246	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	872	736	246	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	869	736	246	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1002;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	618	340	114	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	618	340	114	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=299;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=889;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	472	340	114	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	618	340	114	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	536	457	153	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=27;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=640;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=935;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	986	619	207	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	869	619	207	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	618	259	87	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	618	259	87	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	618	259	87	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	872	619	207	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	926	619	207	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	869	619	207	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
100815	17:7674227-7674227	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	879	619	207	M/V	Atg/Gtg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	878	736	246	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	736	736	246	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	736	736	246	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	869	736	246	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	872	736	246	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	869	736	246	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1002;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	618	340	114	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	618	340	114	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=299;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=889;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	472	340	114	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	618	340	114	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	536	457	153	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=27;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=640;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=935;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	986	619	207	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	869	619	207	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	618	259	87	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	618	259	87	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	618	259	87	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	872	619	207	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	926	619	207	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	869	619	207	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186737	17:7674227-7674227	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	879	619	207	M/L	Atg/Ctg	rs483352695,CM942294,COSV52664850,COSV52707693,COSV52949209,COSV53107767	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	876	734	245	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	734	734	245	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	734	734	245	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	867	734	245	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	870	734	245	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	867	734	245	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1000;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	616	338	113	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	616	338	113	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=297;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	470	338	113	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	616	338	113	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	534	455	152	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=25;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=642;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=933;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	984	617	206	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	867	617	206	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	616	257	86	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	616	257	86	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	616	257	86	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	870	617	206	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	924	617	206	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	867	617	206	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
265357	17:7674229-7674229	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	877	617	206	G/A	gGc/gCc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	876	734	245	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	734	734	245	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	734	734	245	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	867	734	245	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	870	734	245	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	867	734	245	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1000;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	616	338	113	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	616	338	113	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=297;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	470	338	113	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	616	338	113	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	534	455	152	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=25;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=642;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=933;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	984	617	206	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	867	617	206	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	616	257	86	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	616	257	86	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	616	257	86	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	870	617	206	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	924	617	206	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	867	617	206	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12355	17:7674229-7674229	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	877	617	206	G/D	gGc/gAc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	875	733	245	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	733	733	245	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	733	733	245	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	866	733	245	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	869	733	245	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	866	733	245	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=999;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	615	337	113	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	615	337	113	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=296;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=886;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	469	337	113	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	615	337	113	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	533	454	152	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=24;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=643;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=932;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	983	616	206	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	866	616	206	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	615	256	86	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	615	256	86	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	615	256	86	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	869	616	206	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	923	616	206	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	866	616	206	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12349	17:7674230-7674230	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	876	616	206	G/C	Ggc/Tgc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	875	733	245	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	733	733	245	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	733	733	245	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	866	733	245	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	869	733	245	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	866	733	245	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=999;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	615	337	113	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	615	337	113	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=296;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=886;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	469	337	113	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	615	337	113	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	533	454	152	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=24;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=643;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=932;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	983	616	206	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	866	616	206	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	615	256	86	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	615	256	86	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	615	256	86	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	869	616	206	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	923	616	206	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	866	616	206	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12365	17:7674230-7674230	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	876	616	206	G/S	Ggc/Agc	rs28934575,CM010463,CM900210,CM920674,COSV52661744,COSV52661877,COSV52713951,COSV52839866	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	867	725	242	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	725	725	242	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	725	725	242	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	858	725	242	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	861	725	242	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	858	725	242	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=991;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	607	329	110	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	607	329	110	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=288;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=878;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	461	329	110	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	607	329	110	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	525	446	149	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=16;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=651;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=924;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	975	608	203	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	858	608	203	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	607	248	83	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	607	248	83	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	607	248	83	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	861	608	203	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	915	608	203	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	858	608	203	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12354	17:7674238-7674238	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	868	608	203	C/Y	tGc/tAc	rs121912655,CM910618,COSV52661189,COSV52677418,COSV52689710	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	864	722	241	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	722	722	241	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	722	722	241	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	855	722	241	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	858	722	241	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	855	722	241	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=988;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	604	326	109	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	604	326	109	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=285;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=875;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	458	326	109	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	604	326	109	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	522	443	148	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=13;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=654;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=921;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	972	605	202	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	855	605	202	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	604	245	82	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	604	245	82	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	604	245	82	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	858	605	202	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	912	605	202	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	855	605	202	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12359	17:7674241-7674241	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	865	605	202	S/F	tCc/tTc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	864	722	241	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	722	722	241	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	722	722	241	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	855	722	241	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	858	722	241	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	855	722	241	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=988;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	604	326	109	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	604	326	109	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=285;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=875;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	458	326	109	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	604	326	109	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	522	443	148	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=13;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=654;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=921;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	972	605	202	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	855	605	202	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	604	245	82	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	604	245	82	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	604	245	82	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	858	605	202	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	912	605	202	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	855	605	202	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
177791	17:7674241-7674241	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	865	605	202	S/C	tCc/tGc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	855	713	238	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	713	713	238	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	713	713	238	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	846	713	238	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	849	713	238	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	846	713	238	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=979;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	595	317	106	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	595	317	106	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=276;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=866;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	449	317	106	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	595	317	106	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	513	434	145	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=663;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=912;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	963	596	199	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	846	596	199	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	595	236	79	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	595	236	79	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	595	236	79	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	849	596	199	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	903	596	199	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	846	596	199	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182935	17:7674250-7674250	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	856	596	199	C/Y	tGt/tAt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	853	711	237	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	711	711	237	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	711	711	237	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	844	711	237	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	847	711	237	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	844	711	237	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=977;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	593	315	105	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	593	315	105	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=274;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=864;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	447	315	105	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	593	315	105	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	511	432	144	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=665;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=910;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	961	594	198	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	844	594	198	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	593	234	78	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	593	234	78	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	593	234	78	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	847	594	198	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	901	594	198	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	844	594	198	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142714	17:7674252-7674252	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	854	594	198	M/I	atG/atA	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	843	701	234	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	701	701	234	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	701	701	234	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	834	701	234	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	837	701	234	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	834	701	234	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=967;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	583	305	102	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	583	305	102	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=264;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=854;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	437	305	102	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	583	305	102	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	501	422	141	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	96	-	-	-	-	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=675;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=900;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	951	584	195	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	834	584	195	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	583	224	75	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	583	224	75	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	583	224	75	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	837	584	195	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	891	584	195	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	834	584	195	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127820	17:7674262-7674262	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	844	584	195	Y/C	tAc/tGc	rs587780073,CM035576,COSV52661201,COSV52686167,COSV53142556	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	837	695	232	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	695	695	232	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	695	695	232	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	828	695	232	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	831	695	232	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	828	695	232	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=961;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	577	299	100	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	577	299	100	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=258;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=848;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	431	299	100	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	577	299	100	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	495	416	139	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	90	-	-	-	-	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=681;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=894;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	945	578	193	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	828	578	193	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	577	218	73	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	577	218	73	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	577	218	73	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	831	578	193	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	885	578	193	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	828	578	193	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141224	17:7674268-7674268	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	838	578	193	I/T	aTc/aCc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	801	659	220	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	659	659	220	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	659	659	220	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	792	659	220	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	795	659	220	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	792	659	220	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=357;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	541	263	88	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	541	263	88	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	915	-	-	-	-	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=244;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	395	263	88	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	541	263	88	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	459	380	127	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1285;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=290;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	909	542	181	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	792	542	181	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	541	182	61	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	541	182	61	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	541	182	61	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	795	542	181	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	849	542	181	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	792	542	181	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127819	17:7674872-7674872	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	802	542	181	Y/C	tAt/tGt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	801	659	220	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	659	659	220	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	659	659	220	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	792	659	220	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	795	659	220	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	792	659	220	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=357;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	541	263	88	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	541	263	88	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	915	-	-	-	-	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=244;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	395	263	88	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	541	263	88	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	459	380	127	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1285;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=290;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	909	542	181	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	792	542	181	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	541	182	61	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	541	182	61	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	541	182	61	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	795	542	181	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	849	542	181	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	792	542	181	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
12383	17:7674872-7674872	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	802	542	181	Y/S	tAt/tCt	rs121912666,CM015378,CM951227,COSV52661282,COSV52677517	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	780	638	213	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	638	638	213	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	638	638	213	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	771	638	213	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	774	638	213	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	771	638	213	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=336;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	520	242	81	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	520	242	81	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	894	-	-	-	-	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=223;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	374	242	81	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	520	242	81	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	438	359	120	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1306;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=269;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	888	521	174	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	771	521	174	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	520	161	54	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	520	161	54	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	520	161	54	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	774	521	174	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	828	521	174	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	771	521	174	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231214	17:7674893-7674893	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	781	521	174	R/P	cGa/cCa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	780	638	213	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	638	638	213	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	638	638	213	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	771	638	213	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	774	638	213	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	771	638	213	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=336;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	520	242	81	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	520	242	81	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	894	-	-	-	-	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=223;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	374	242	81	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	520	242	81	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	438	359	120	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1306;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=269;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	888	521	174	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	771	521	174	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	520	161	54	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	520	161	54	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	520	161	54	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	774	521	174	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	828	521	174	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	771	521	174	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
135359	17:7674893-7674893	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	781	521	174	R/Q	cGa/cAa	rs587778720,CM004906,CM022474,COSV52665093,COSV52668963,COSV52693072	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	726	584	195	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	584	584	195	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	584	584	195	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	717	584	195	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	720	584	195	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	717	584	195	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=282;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	466	188	63	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	466	188	63	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	840	-	-	-	-	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=169;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	320	188	63	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	466	188	63	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	384	305	102	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1360;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=215;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	834	467	156	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	717	467	156	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	466	107	36	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	466	107	36	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	466	107	36	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	720	467	156	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	774	467	156	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	717	467	156	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
216077	17:7674947-7674947	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	727	467	156	I/T	aTc/aCc	rs760043106,CM092575,COSV52661172,COSV52664264,COSV52684176,COSV52720899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	722	580	194	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	580	580	194	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	580	580	194	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	713	580	194	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	716	580	194	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	713	580	194	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=278;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	462	184	62	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	462	184	62	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	836	-	-	-	-	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=165;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	316	184	62	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	462	184	62	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	380	301	101	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1364;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=211;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	830	463	155	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	713	463	155	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	462	103	35	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	462	103	35	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	462	103	35	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	716	463	155	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	770	463	155	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	713	463	155	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127817	17:7674951-7674951	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	723	463	155	L/F	Ctt/Ttt	rs587780071,CM120848,COSV52677226,COSV52796536,COSV53623808	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	720	578	193	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	578	578	193	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	578	578	193	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	711	578	193	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	714	578	193	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	711	578	193	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=276;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	460	182	61	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	460	182	61	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	834	-	-	-	-	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=163;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	314	182	61	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	460	182	61	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	378	299	100	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1366;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=209;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	828	461	154	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	711	461	154	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	460	101	34	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	460	101	34	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	460	101	34	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	714	461	154	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	768	461	154	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	711	461	154	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
184979	17:7674953-7674953	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	721	461	154	H/R	cAt/cGt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	719	577	193	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	577	577	193	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	577	577	193	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	710	577	193	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	713	577	193	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	710	577	193	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=275;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	459	181	61	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	459	181	61	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	833	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=162;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	313	181	61	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	459	181	61	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	377	298	100	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1367;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=208;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	827	460	154	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	710	460	154	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	459	100	34	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	459	100	34	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	459	100	34	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	713	460	154	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	767	460	154	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	710	460	154	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230256	17:7674954-7674954	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	720	460	154	H/Y	Cat/Tat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	680	538	180	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	538	538	180	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	538	538	180	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	671	538	180	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	674	538	180	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	671	538	180	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=155;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	420	142	48	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	420	142	48	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	794	-	-	-	-	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=42;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	274	142	48	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	420	142	48	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	338	259	87	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	46	-	-	-	-	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1487;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=88;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	788	421	141	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	671	421	141	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	420	61	21	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	420	61	21	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	420	61	21	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	674	421	141	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	728	421	141	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	671	421	141	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
245711	17:7675074-7675074	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	681	421	141	E/K	Gag/Aag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	677	535	179	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	535	535	179	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	535	535	179	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	668	535	179	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	671	535	179	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	668	535	179	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=152;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	417	139	47	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	417	139	47	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	791	-	-	-	-	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=39;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	271	139	47	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	417	139	47	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	335	256	86	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	43	-	-	-	-	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1490;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=85;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	785	418	140	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	668	418	140	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	417	58	20	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	417	58	20	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	417	58	20	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	671	418	140	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	725	418	140	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	668	418	140	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127815	17:7675077-7675077	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	678	418	140	H/Y	Cat/Tat	rs587780070,CM067054,COSV52662617,COSV52668276,COSV52699993	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	669	527	176	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	527	527	176	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	527	527	176	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	660	527	176	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	663	527	176	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	660	527	176	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=144;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	409	131	44	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	409	131	44	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	783	-	-	-	-	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=31;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	263	131	44	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	409	131	44	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	327	248	83	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	35	-	-	-	-	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1498;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=77;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	777	410	137	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	660	410	137	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	409	50	17	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	409	50	17	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	409	50	17	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	663	410	137	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	717	410	137	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	660	410	137	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186451	17:7675085-7675085	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	670	410	137	C/Y	tGc/tAc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	666	524	175	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	524	524	175	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	524	524	175	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	657	524	175	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	660	524	175	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	657	524	175	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=141;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	406	128	43	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	406	128	43	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	780	-	-	-	-	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=28;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	260	128	43	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	406	128	43	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	324	245	82	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	32	-	-	-	-	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1501;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=74;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	774	407	136	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	657	407	136	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	406	47	16	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	406	47	16	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	406	47	16	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	660	407	136	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	714	407	136	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	657	407	136	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
182963	17:7675088-7675088	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	667	407	136	R/L	cGc/cTc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	666	524	175	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	524	524	175	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	524	524	175	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	657	524	175	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	660	524	175	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	657	524	175	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=141;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	406	128	43	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	406	128	43	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	780	-	-	-	-	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=28;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	260	128	43	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	406	128	43	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	324	245	82	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	32	-	-	-	-	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1501;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=74;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	774	407	136	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	657	407	136	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	406	47	16	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	406	47	16	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	406	47	16	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	660	407	136	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	714	407	136	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	657	407	136	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12374	17:7675088-7675088	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	667	407	136	R/H	cGc/cAc	rs28934578,CM062017,CM951224,COSV52661038,COSV52677601,COSV52731306,COSV53801286	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	659	517	173	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	517	517	173	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	517	517	173	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	650	517	173	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	653	517	173	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	650	517	173	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=134;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	399	121	41	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	399	121	41	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	773	-	-	-	-	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=21;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	253	121	41	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	399	121	41	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	317	238	80	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	25	-	-	-	-	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1508;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=67;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	767	400	134	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	650	400	134	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	399	40	14	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	399	40	14	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	399	40	14	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	653	400	134	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	707	400	134	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	650	400	134	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
233951	17:7675095-7675095	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	660	400	134	V/M	Gtg/Atg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	630	488	163	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	488	488	163	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	488	488	163	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	621	488	163	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	624	488	163	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	621	488	163	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=105;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	370	92	31	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	370	92	31	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	744	-	-	-	-	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	626	488	163	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	224	92	31	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	370	92	31	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	288	209	70	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1537;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=38;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	738	371	124	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	621	371	124	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	370	11	4	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	370	11	4	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	370	11	4	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	624	371	124	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	678	371	124	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	621	371	124	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
127814	17:7675124-7675124	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	631	371	124	Y/C	tAc/tGc	rs148924904,CM942135,COSV52663142,COSV52676381	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	615	473	158	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	473	473	158	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	473	473	158	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	606	473	158	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	609	473	158	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	606	473	158	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=90;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	355	77	26	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	355	77	26	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	729	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	611	473	158	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	209	77	26	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	355	77	26	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	273	194	65	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=20;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1552;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=23;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	723	356	119	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	606	356	119	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	355	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	355	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	355	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	609	356	119	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	663	356	119	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	606	356	119	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
246118	17:7675139-7675139	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	616	356	119	R/P	cGc/cCc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	615	473	158	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	473	473	158	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	473	473	158	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	606	473	158	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	609	473	158	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	606	473	158	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=90;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	355	77	26	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	355	77	26	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	729	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	611	473	158	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	209	77	26	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	355	77	26	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	273	194	65	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=20;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1552;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=23;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	723	356	119	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	606	356	119	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	355	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	355	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	355	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	609	356	119	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	663	356	119	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	606	356	119	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
141963	17:7675139-7675139	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	616	356	119	R/H	cGc/cAc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	597	455	152	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	455	455	152	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	455	455	152	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	588	455	152	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	591	455	152	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	588	455	152	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=72;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	337	59	20	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	337	59	20	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	711	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	593	455	152	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	191	59	20	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	337	59	20	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	255	176	59	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=38;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1570;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	705	338	113	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	588	338	113	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	337	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	337	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	337	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	591	338	113	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	645	338	113	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	588	338	113	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
142766	17:7675157-7675157	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	598	338	113	P/L	cCg/cTg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	593	451	151	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	451	451	151	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	451	451	151	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	584	451	151	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	587	451	151	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	584	451	151	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=68;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	333	55	19	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	333	55	19	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	707	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	589	451	151	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	187	55	19	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	333	55	19	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	251	172	58	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=42;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1574;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	701	334	112	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	584	334	112	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	333	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	333	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	333	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	587	334	112	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	641	334	112	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	584	334	112	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12370	17:7675161-7675161	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	594	334	112	P/S	Ccc/Tcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	593	451	151	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	451	451	151	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	451	451	151	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	584	451	151	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	587	451	151	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	584	451	151	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=68;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	333	55	19	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	333	55	19	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	707	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	589	451	151	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	187	55	19	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	333	55	19	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	251	172	58	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=42;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1574;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	701	334	112	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	584	334	112	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	333	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	333	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	333	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	587	334	112	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	641	334	112	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	584	334	112	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12369	17:7675161-7675161	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	594	334	112	P/T	Ccc/Acc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	564	422	141	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	422	422	141	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	422	422	141	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	555	422	141	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	558	422	141	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	555	422	141	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=39;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	304	26	9	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	304	26	9	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	678	-	-	-	-	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	560	422	141	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	158	26	9	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	304	26	9	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	222	143	48	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=71;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1603;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	540	401	134	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	672	305	102	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	555	305	102	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	304	-	-	-	-	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	304	-	-	-	-	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	304	-	-	-	-	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	558	305	102	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	612	305	102	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	555	305	102	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
140801	17:7675190-7675190	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	565	305	102	C/Y	tGc/tAc	rs587781288,CM993216,COSV52664953,COSV52926626,COSV53155598	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	554	412	138	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	412	412	138	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	412	412	138	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	545	412	138	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	548	412	138	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	545	412	138	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=29;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	294	16	6	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	294	16	6	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	668	-	-	-	-	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	550	412	138	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	148	16	6	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	294	16	6	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	212	133	45	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=81;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1613;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	530	391	131	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	662	295	99	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	545	295	99	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	294	-	-	-	-	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	294	-	-	-	-	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	294	-	-	-	-	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	548	295	99	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	602	295	99	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	545	295	99	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12376	17:7675200-7675200	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	555	295	99	A/P	Gcc/Ccc	rs28934875,CM942116,CM983475,COSV52661607,COSV52839281,COSV53396164	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	543	401	134	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	401	401	134	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	401	401	134	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	534	401	134	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	537	401	134	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	534	401	134	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=18;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	283	5	2	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	283	5	2	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	657	-	-	-	-	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	539	401	134	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	137	5	2	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	283	5	2	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	201	122	41	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=92;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1624;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	519	380	127	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	651	284	95	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	534	284	95	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	283	-	-	-	-	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	283	-	-	-	-	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	283	-	-	-	-	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	537	284	95	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	591	284	95	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	534	284	95	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
230477	17:7675211-7675211	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	544	284	95	F/C	tTt/tGt	rs780442292,CM083195,COSV52669400,COSV52722353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	540	398	133	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	398	398	133	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	398	398	133	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	531	398	133	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	534	398	133	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	531	398	133	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=15;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000504290.5	Transcript	start_lost	280	2	1	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000504937.5	Transcript	start_lost	280	2	1	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	654	-	-	-	-	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	536	398	133	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000509690.5	Transcript	start_lost	134	2	1	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000510385.5	Transcript	start_lost	280	2	1	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	198	119	40	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=95;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1627;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant,splice_region_variant	516	377	126	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	648	281	94	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	531	281	94	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	280	-	-	-	-	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	280	-	-	-	-	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	280	-	-	-	-	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	534	281	94	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	588	281	94	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	531	281	94	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
12357	17:7675214-7675214	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	541	281	94	M/T	aTg/aCg	rs28934873,CM910373,CM973400,COSV52744834,COSV52795528,COSV52821486,COSV52852024	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	533	391	131	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	391	391	131	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	391	391	131	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	524	391	131	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	527	391	131	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	524	391	131	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=8;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	273	-	-	-	-	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	273	-	-	-	-	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	647	-	-	-	-	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	529	391	131	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	127	-	-	-	-	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	273	-	-	-	-	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	191	112	38	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=102;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1634;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	641	274	92	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	524	274	92	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	273	-	-	-	-	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	273	-	-	-	-	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	273	-	-	-	-	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	527	274	92	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	581	274	92	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	524	274	92	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141988	17:7675221-7675221	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	534	274	92	N/Y	Aac/Tac	rs587782160,COSV52788120,COSV53200449,COSV53325650	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant,splice_region_variant	516	374	125	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant,splice_region_variant	374	374	125	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant,splice_region_variant	374	374	125	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant,splice_region_variant	507	374	125	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant,splice_region_variant	510	374	125	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant,splice_region_variant	507	374	125	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant,splice_region_variant	556	374	125	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	630	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant,splice_region_variant	512	374	125	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=876;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2408;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant,splice_region_variant	513	374	125	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant,splice_region_variant	624	257	86	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant,splice_region_variant	507	257	86	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant,splice_region_variant	510	257	86	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant,splice_region_variant	564	257	86	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant,splice_region_variant	507	257	86	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
216465	17:7675995-7675995	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,splice_region_variant,NMD_transcript_variant	517	257	86	T/K	aCg/aAg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	471	329	110	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	329	329	110	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	329	329	110	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	462	329	110	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	465	329	110	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	462	329	110	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	511	329	110	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	585	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	467	329	110	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=921;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2453;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	468	329	110	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	579	212	71	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	462	212	71	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	465	212	71	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	519	212	71	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	462	212	71	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
233627	17:7676040-7676040	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	472	212	71	R/P	cGt/cCt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	247	105	35	L/F	ttG/ttT	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	105	105	35	L/F	ttG/ttT	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	105	105	35	L/F	ttG/ttT	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	238	105	35	L/F	ttG/ttT	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	241	105	35	L/F	ttG/ttT	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	238	105	35	L/F	ttG/ttT	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	287	105	35	L/F	ttG/ttT	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	361	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	243	105	35	L/F	ttG/ttT	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1145;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2677;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	244	105	35	L/F	ttG/ttT	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	355	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	238	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	241	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	295	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	238	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
12371	17:7676264-7676264	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	248	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=218;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=201;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=218;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=201;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=199;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=199;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=199;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1366;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=199;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=201;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=199;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=199;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=199;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=218;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=199;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=201;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
437018	17:7668202-7668202	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555523630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,stop_retained_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	124-1345	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-11/11;INTRON=2-10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-8/9;INTRON=1-8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-6/7;INTRON=1-6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,stop_retained_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	115-1469	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-12/12;INTRON=2-11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,stop_retained_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	118-1339	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-11/11;INTRON=2-10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,stop_retained_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	115-1396	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-12/12;INTRON=2-11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	164-?	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3-6/6;INTRON=3-5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	?-1145	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-8/8;INTRON=1-7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	?-1085	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-7/7;INTRON=1-6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,non_coding_transcript_exon_variant,intron_variant	121-?	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2-5/5;INTRON=2-4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	120-?	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-5/5;INTRON=2-4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-6/6;INTRON=1-5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	?-1218	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-8/8;INTRON=1-7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	61-?	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-6/6;INTRON=2-5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000574684.1	Transcript	transcript_ablation	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1-2/2;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000576024.1	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	?-156	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-2/2;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	121-?	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-5/5;INTRON=2-4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,stop_retained_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	115-1453	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-10/10;INTRON=2-9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,stop_retained_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	115-1396	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-12/12;INTRON=2-11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	?-1145	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-8/8;INTRON=1-7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	?-1218	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-8/8;INTRON=1-7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	?-1085	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-7/7;INTRON=1-6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,stop_retained_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	118-1339	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-11/11;INTRON=2-10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,stop_retained_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	172-1393	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-11/11;INTRON=2-10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,stop_retained_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant	115-1469	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-12/12;INTRON=2-11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant,NMD_transcript_variant	125-?	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2-10/12;INTRON=2-10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1174011	17:7669587-7676613	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_ablation,regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
1174011	17:7669587-7676613	-	-	ENSR00000548581	RegulatoryFeature	regulatory_region_ablation,regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=TF_binding_site
1174011	17:7669587-7676613	-	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=enhancer
1174011	17:7669587-7676613	-	-	ENSM00000008967	MotifFeature	TFBS_ablation,TF_binding_site_variant	-	-	-	-	-	-	IMPACT=MODERATE;STRAND=1;MOTIF_NAME=ENSPFM0042;HIGH_INF_POS=N;TRANSCRIPTION_FACTORS=CTCF
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1267	1125	375	Q/X	caG/ca	rs730882017,CD1617857,COSV105874506	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1391	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1261	1125	375	Q/X	caG/ca	rs730882017,CD1617857,COSV105874506	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1318	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1067	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	1007	729	243	Q/X	caG/ca	rs730882017,CD1617857,COSV105874506	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4860;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3869;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1140	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4551;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	78	79	27	V/X	Gtc/tc	rs730882017,CD1617857,COSV105874506	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1375	1008	336	Q/X	caG/ca	rs730882017,CD1617857,COSV105874506	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1318	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1067	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1140	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	1007	648	216	Q/X	caG/ca	rs730882017,CD1617857,COSV105874506	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1261	1008	336	Q/X	caG/ca	rs730882017,CD1617857,COSV105874506	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1315	1008	336	Q/X	caG/ca	rs730882017,CD1617857,COSV105874506	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1391	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182956	17:7669665-7669666	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs730882017,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4835;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3844;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4526;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000576024.1	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
231146	17:7669691-7669691	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs876658982,COSV53196286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,not_provided;SOMATIC=0,1;PHENO=1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4834;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3843;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4525;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000576024.1	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141332	17:7669692-7669692	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs587781664,CS111031,COSV52676811,COSV52714663,COSV53348267	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV105029802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV105029802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105029802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4622;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105029802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3919;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105029802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4509;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105029802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2928;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105029802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3610;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105029802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3647;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	COSV105029802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105029802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4555;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1525255	17:7670607-7670607	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	COSV105029802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1225	1083	361	G/X	ggG/gg	rs1555524354,COSV53093481	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1349	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1219	1083	361	G/X	ggG/gg	rs1555524354,COSV53093481	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1276	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4603;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1025	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	965	687	229	G/X	ggG/gg	rs1555524354,COSV53093481	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3900;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4490;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2909;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1098	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3591;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3628;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4536;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1333	966	322	G/X	ggG/gg	rs1555524354,COSV53093481	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1276	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1025	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1098	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	965	606	202	G/X	ggG/gg	rs1555524354,COSV53093481	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1219	966	322	G/X	ggG/gg	rs1555524354,COSV53093481	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1273	966	322	G/X	ggG/gg	rs1555524354,COSV53093481	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1349	-	-	-	-	rs1555524354,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549856	17:7670625-7670626	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1226	966	322	G/X	ggG/gg	rs1555524354,COSV53093481	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1219	1077	359	P/X	ccA/cc	rs1555524370	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1343	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1213	1077	359	P/X	ccA/cc	rs1555524370	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1270	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4597;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1019	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	959	681	227	P/X	ccA/cc	rs1555524370	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3894;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4484;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2903;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1092	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3585;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3622;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4530;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1327	960	320	P/X	ccA/cc	rs1555524370	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1270	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1019	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1092	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	959	600	200	P/X	ccA/cc	rs1555524370	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1213	960	320	P/X	ccA/cc	rs1555524370	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1267	960	320	P/X	ccA/cc	rs1555524370	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1343	-	-	-	-	rs1555524370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
549855	17:7670631-7670632	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1220	960	320	P/X	ccA/cc	rs1555524370	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1202	1060	354	Q/*	Cag/Tag	rs755394212,COSV52783779,COSV53018657	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1326	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1196	1060	354	Q/*	Cag/Tag	rs755394212,COSV52783779,COSV53018657	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1253	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4580;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1002	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	942	664	222	Q/*	Cag/Tag	rs755394212,COSV52783779,COSV53018657	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3877;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4467;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2886;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1075	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3568;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3605;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4513;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1310	943	315	Q/*	Cag/Tag	rs755394212,COSV52783779,COSV53018657	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1253	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1002	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1075	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	942	583	195	Q/*	Cag/Tag	rs755394212,COSV52783779,COSV53018657	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1196	943	315	Q/*	Cag/Tag	rs755394212,COSV52783779,COSV53018657	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1250	943	315	Q/*	Cag/Tag	rs755394212,COSV52783779,COSV53018657	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1326	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458514	17:7670649-7670649	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1203	943	315	Q/*	Cag/Tag	rs755394212,COSV52783779,COSV53018657	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1188-1197	1046-1055	349-352	ELKD/X	gAACTCAAGGAt/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1312-1321	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1182-1191	1046-1055	349-352	ELKD/X	gAACTCAAGGAt/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1239-1248	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4566;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	988-997	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	928-937	650-659	217-220	ELKD/X	gAACTCAAGGAt/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3863;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4453;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2872;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1061-1070	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3554;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3591;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4499;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1296-1305	929-938	310-313	ELKD/X	gAACTCAAGGAt/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1239-1248	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	988-997	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1061-1070	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	928-937	569-578	190-193	ELKD/X	gAACTCAAGGAt/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1182-1191	929-938	310-313	ELKD/X	gAACTCAAGGAt/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1236-1245	929-938	310-313	ELKD/X	gAACTCAAGGAt/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1312-1321	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505686	17:7670653-7670663	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1189-1198	929-938	310-313	ELKD/X	gAACTCAAGGAt/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1196	1054	352	D/X	Gat/at	COSV99405827	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1320	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1190	1054	352	D/X	Gat/at	COSV99405827	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1247	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4574;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	996	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	936	658	220	D/X	Gat/at	COSV99405827	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3871;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4461;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2880;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1069	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3562;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4507;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1304	937	313	D/X	Gat/at	COSV99405827	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1247	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	996	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1069	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	936	577	193	D/X	Gat/at	COSV99405827	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1190	937	313	D/X	Gat/at	COSV99405827	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1244	937	313	D/X	Gat/at	COSV99405827	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1320	-	-	-	-	COSV99405827	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1505744	17:7670654-7670655	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1197	937	313	D/X	Gat/at	COSV99405827	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1194	1052	351	K/X	aAg/ag	COSV53304065	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1318	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1188	1052	351	K/X	aAg/ag	COSV53304065	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1245	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4572;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	994	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	934	656	219	K/X	aAg/ag	COSV53304065	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3869;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4459;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2878;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1067	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3560;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4505;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1302	935	312	K/X	aAg/ag	COSV53304065	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1245	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	994	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1067	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	934	575	192	K/X	aAg/ag	COSV53304065	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1188	935	312	K/X	aAg/ag	COSV53304065	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1242	935	312	K/X	aAg/ag	COSV53304065	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1318	-	-	-	-	COSV53304065	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066207	17:7670656-7670657	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1195	935	312	K/X	aAg/ag	COSV53304065	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1191-1192	1049-1050	350	L/X	cTC/c	rs1131691008	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1315-1316	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1185-1186	1049-1050	350	L/X	cTC/c	rs1131691008	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1242-1243	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4569;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	991-992	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	931-932	653-654	218	L/X	cTC/c	rs1131691008	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3866;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4456;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2875;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1064-1065	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3557;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4502;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1299-1300	932-933	311	L/X	cTC/c	rs1131691008	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1242-1243	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	991-992	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1064-1065	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	931-932	572-573	191	L/X	cTC/c	rs1131691008	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1185-1186	932-933	311	L/X	cTC/c	rs1131691008	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1239-1240	932-933	311	L/X	cTC/c	rs1131691008	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1315-1316	-	-	-	-	rs1131691008	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428864	17:7670658-7670660	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1192-1193	932-933	311	L/X	cTC/c	rs1131691008	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained,frameshift_variant	1185-1193	1043-1051	348-351	LELK/*	tTGGAACTCAag/tGag	rs1567541951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1309-1317	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained,frameshift_variant	1179-1187	1043-1051	348-351	LELK/*	tTGGAACTCAag/tGag	rs1567541951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1236-1244	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4563;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	985-993	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained,frameshift_variant	925-933	647-655	216-219	LELK/*	tTGGAACTCAag/tGag	rs1567541951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3860;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4450;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2869;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1058-1066	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3551;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4496;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained,frameshift_variant	1293-1301	926-934	309-312	LELK/*	tTGGAACTCAag/tGag	rs1567541951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1236-1244	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	985-993	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1058-1066	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained,frameshift_variant	925-933	566-574	189-192	LELK/*	tTGGAACTCAag/tGag	rs1567541951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained,frameshift_variant	1179-1187	926-934	309-312	LELK/*	tTGGAACTCAag/tGag	rs1567541951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained,frameshift_variant	1233-1241	926-934	309-312	LELK/*	tTGGAACTCAag/tGag	rs1567541951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1309-1317	-	-	-	-	rs1567541951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
576681	17:7670658-7670666	C	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,frameshift_variant,NMD_transcript_variant	1186-1194	926-934	309-312	LELK/*	tTGGAACTCAag/tGag	rs1567541951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1187	1045	349	E/*	Gaa/Taa	rs1567541975,COSV52696505	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1311	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1181	1045	349	E/*	Gaa/Taa	rs1567541975,COSV52696505	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1238	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4565;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	987	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	927	649	217	E/*	Gaa/Taa	rs1567541975,COSV52696505	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3862;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4452;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2871;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1060	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3553;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3590;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4498;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1295	928	310	E/*	Gaa/Taa	rs1567541975,COSV52696505	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1238	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	987	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1060	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	927	568	190	E/*	Gaa/Taa	rs1567541975,COSV52696505	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1181	928	310	E/*	Gaa/Taa	rs1567541975,COSV52696505	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1235	928	310	E/*	Gaa/Taa	rs1567541975,COSV52696505	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1311	-	-	-	-	rs1567541975,COSV52696505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634695	17:7670664-7670664	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1188	928	310	E/*	Gaa/Taa	rs1567541975,COSV52696505	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1185	1043	348	L/X	tTg/tg	COSV52736234,COSV53072454,COSV99425698	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1309	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1179	1043	348	L/X	tTg/tg	COSV52736234,COSV53072454,COSV99425698	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1236	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4563;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	985	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	925	647	216	L/X	tTg/tg	COSV52736234,COSV53072454,COSV99425698	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3860;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4450;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2869;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1058	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3551;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4496;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1293	926	309	L/X	tTg/tg	COSV52736234,COSV53072454,COSV99425698	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1236	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	985	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1058	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	925	566	189	L/X	tTg/tg	COSV52736234,COSV53072454,COSV99425698	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1179	926	309	L/X	tTg/tg	COSV52736234,COSV53072454,COSV99425698	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1233	926	309	L/X	tTg/tg	COSV52736234,COSV53072454,COSV99425698	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1309	-	-	-	-	COSV52736234,COSV53072454,COSV99425698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1066930	17:7670665-7670666	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1186	926	309	L/X	tTg/tg	COSV52736234,COSV53072454,COSV99425698	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1182	1040	347	A/D	gCc/gAc	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1306	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1176	1040	347	A/D	gCc/gAc	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1233	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4560;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	982	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	922	644	215	A/D	gCc/gAc	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3857;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4447;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2866;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1055	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3548;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3585;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4493;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1290	923	308	A/D	gCc/gAc	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1233	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	982	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1055	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	922	563	188	A/D	gCc/gAc	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1176	923	308	A/D	gCc/gAc	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1230	923	308	A/D	gCc/gAc	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1306	-	-	-	-	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
43587	17:7670669-7670669	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1183	923	308	A/D	gCc/gAc	rs397516434,CD016207,CM169324,COSV53328077,COSV53408022,COSV53835207,COSV99037318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1178	1036	346	E/X	Gag/ag	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1302	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1172	1036	346	E/X	Gag/ag	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1229	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4556;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	978	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	918	640	214	E/X	Gag/ag	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3853;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4443;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2862;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1051	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3544;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3581;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4489;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1286	919	307	E/X	Gag/ag	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1229	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	978	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1051	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	918	559	187	E/X	Gag/ag	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1172	919	307	E/X	Gag/ag	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1226	919	307	E/X	Gag/ag	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1302	-	-	-	-	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634693	17:7670672-7670673	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1179	919	307	E/X	Gag/ag	rs1567542031,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1178	1036	346	E/*	Gag/Tag	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1302	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1172	1036	346	E/*	Gag/Tag	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1229	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4556;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	978	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	918	640	214	E/*	Gag/Tag	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3853;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4443;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2862;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1051	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3544;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3581;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4489;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1286	919	307	E/*	Gag/Tag	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1229	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	978	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1051	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	918	559	187	E/*	Gag/Tag	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1172	919	307	E/*	Gag/Tag	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1226	919	307	E/*	Gag/Tag	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1302	-	-	-	-	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634697	17:7670673-7670673	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1179	919	307	E/*	Gag/Tag	rs1567542019,CM123558,COSV52688134,COSV99393932	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1169-1176	1027-1034	343-345	ELN/X	GAGCTGAAt/t	rs1567542043	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1293-1300	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1163-1170	1027-1034	343-345	ELN/X	GAGCTGAAt/t	rs1567542043	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1220-1227	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4547;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	969-976	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	909-916	631-638	211-213	ELN/X	GAGCTGAAt/t	rs1567542043	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3844;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4434;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2853;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1042-1049	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3535;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3572;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4480;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1277-1284	910-917	304-306	ELN/X	GAGCTGAAt/t	rs1567542043	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1220-1227	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	969-976	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1042-1049	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	909-916	550-557	184-186	ELN/X	GAGCTGAAt/t	rs1567542043	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1163-1170	910-917	304-306	ELN/X	GAGCTGAAt/t	rs1567542043	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1217-1224	910-917	304-306	ELN/X	GAGCTGAAt/t	rs1567542043	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1293-1300	-	-	-	-	rs1567542043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634751	17:7670674-7670682	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1170-1177	910-917	304-306	ELN/X	GAGCTGAAt/t	rs1567542043	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1170	1028	343	E/X	gAg/gg	COSV52822268,COSV99436358	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1294	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1164	1028	343	E/X	gAg/gg	COSV52822268,COSV99436358	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1221	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4548;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	970	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	910	632	211	E/X	gAg/gg	COSV52822268,COSV99436358	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3845;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4435;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2854;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1043	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3536;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3573;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4481;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1278	911	304	E/X	gAg/gg	COSV52822268,COSV99436358	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1221	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	970	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1043	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	910	551	184	E/X	gAg/gg	COSV52822268,COSV99436358	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1164	911	304	E/X	gAg/gg	COSV52822268,COSV99436358	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1218	911	304	E/X	gAg/gg	COSV52822268,COSV99436358	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1294	-	-	-	-	COSV52822268,COSV99436358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1698604	17:7670680-7670681	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1171	911	304	E/X	gAg/gg	COSV52822268,COSV99436358	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1161-1170	1019-1028	340-343	MFRE/X	aTGTTCCGAGAg/ag	rs1597349257	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1285-1294	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1155-1164	1019-1028	340-343	MFRE/X	aTGTTCCGAGAg/ag	rs1597349257	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1212-1221	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4539;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	961-970	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	901-910	623-632	208-211	MFRE/X	aTGTTCCGAGAg/ag	rs1597349257	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3836;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4426;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2845;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1034-1043	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3527;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3564;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4472;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1269-1278	902-911	301-304	MFRE/X	aTGTTCCGAGAg/ag	rs1597349257	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1212-1221	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	961-970	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1034-1043	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	901-910	542-551	181-184	MFRE/X	aTGTTCCGAGAg/ag	rs1597349257	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1155-1164	902-911	301-304	MFRE/X	aTGTTCCGAGAg/ag	rs1597349257	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1209-1218	902-911	301-304	MFRE/X	aTGTTCCGAGAg/ag	rs1597349257	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1285-1294	-	-	-	-	rs1597349257	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
818260	17:7670680-7670690	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1162-1171	902-911	301-304	MFRE/X	aTGTTCCGAGAg/ag	rs1597349257	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1166	1024	342	R/X	Cga/ga	rs1131691022,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1290	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1160	1024	342	R/X	Cga/ga	rs1131691022,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1217	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4544;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	966	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	906	628	210	R/X	Cga/ga	rs1131691022,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3841;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4431;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2850;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1039	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3532;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3569;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4477;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1274	907	303	R/X	Cga/ga	rs1131691022,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1217	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	966	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1039	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	906	547	183	R/X	Cga/ga	rs1131691022,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1160	907	303	R/X	Cga/ga	rs1131691022,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1214	907	303	R/X	Cga/ga	rs1131691022,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1290	-	-	-	-	rs1131691022,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428885	17:7670684-7670685	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1167	907	303	R/X	Cga/ga	rs1131691022,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1166	1024	342	R/*	Cga/Tga	rs730882029,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1290	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1160	1024	342	R/*	Cga/Tga	rs730882029,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1217	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4544;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	966	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	906	628	210	R/*	Cga/Tga	rs730882029,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3841;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4431;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2850;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1039	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3532;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3569;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4477;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1274	907	303	R/*	Cga/Tga	rs730882029,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1217	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	966	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1039	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	906	547	183	R/*	Cga/Tga	rs730882029,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1160	907	303	R/*	Cga/Tga	rs730882029,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1214	907	303	R/*	Cga/Tga	rs730882029,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1290	-	-	-	-	rs730882029,CM004908,COSV52665487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
182970	17:7670685-7670685	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1167	907	303	R/*	Cga/Tga	rs730882029,CM004908,COSV52665487	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1163	1021	341	F/EX	Ttc/GAAtc	COSV53651123,COSV99427375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1287	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1157	1021	341	F/EX	Ttc/GAAtc	COSV53651123,COSV99427375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1214	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4541;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	963	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	903	625	209	F/EX	Ttc/GAAtc	COSV53651123,COSV99427375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3838;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4428;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2847;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1036	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3529;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4474;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1271	904	302	F/EX	Ttc/GAAtc	COSV53651123,COSV99427375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1214	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	963	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1036	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	903	544	182	F/EX	Ttc/GAAtc	COSV53651123,COSV99427375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1157	904	302	F/EX	Ttc/GAAtc	COSV53651123,COSV99427375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1211	904	302	F/EX	Ttc/GAAtc	COSV53651123,COSV99427375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1287	-	-	-	-	COSV53651123,COSV99427375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
971781	17:7670688-7670688	TTC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1164	904	302	F/EX	Ttc/GAAtc	COSV53651123,COSV99427375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1160	1018	340	M/X	Atg/tg	rs1131691005,COSV53461649,COSV53588660	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1284	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1154	1018	340	M/X	Atg/tg	rs1131691005,COSV53461649,COSV53588660	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1211	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4538;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	960	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	900	622	208	M/X	Atg/tg	rs1131691005,COSV53461649,COSV53588660	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3835;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4425;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2844;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1033	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3526;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4471;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1268	901	301	M/X	Atg/tg	rs1131691005,COSV53461649,COSV53588660	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1211	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	960	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1033	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	900	541	181	M/X	Atg/tg	rs1131691005,COSV53461649,COSV53588660	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1154	901	301	M/X	Atg/tg	rs1131691005,COSV53461649,COSV53588660	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1208	901	301	M/X	Atg/tg	rs1131691005,COSV53461649,COSV53588660	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1284	-	-	-	-	rs1131691005,COSV53461649,COSV53588660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428861	17:7670690-7670691	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1161	901	301	M/X	Atg/tg	rs1131691005,COSV53461649,COSV53588660	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1156-1157	1014-1015	338-339	-/X	-/C	COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1280-1281	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1150-1151	1014-1015	338-339	-/X	-/C	COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1207-1208	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4534;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	956-957	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	896-897	618-619	206-207	-/X	-/C	COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3831;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4421;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2840;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1029-1030	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3522;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3559;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4467;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1264-1265	897-898	299-300	-/X	-/C	COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1207-1208	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	956-957	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1029-1030	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	896-897	537-538	179-180	-/X	-/C	COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1150-1151	897-898	299-300	-/X	-/C	COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1204-1205	897-898	299-300	-/X	-/C	COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1280-1281	-	-	-	-	COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1072958	17:7670694-7670694	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1157-1158	897-898	299-300	-/X	-/C	COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1157	1015	339	E/*	Gag/Tag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1281	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1151	1015	339	E/*	Gag/Tag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1208	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4535;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	957	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	897	619	207	E/*	Gag/Tag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4422;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2841;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1030	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3523;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3560;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4468;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1265	898	300	E/*	Gag/Tag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1208	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	957	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1030	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	897	538	180	E/*	Gag/Tag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1151	898	300	E/*	Gag/Tag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1205	898	300	E/*	Gag/Tag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1281	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
438708	17:7670694-7670694	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1158	898	300	E/*	Gag/Tag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1156-1157	1014-1015	338-339	-/X	-/T	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1280-1281	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1150-1151	1014-1015	338-339	-/X	-/T	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1207-1208	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4534;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	956-957	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	896-897	618-619	206-207	-/X	-/T	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3831;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4421;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2840;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1029-1030	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3522;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3559;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4467;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1264-1265	897-898	299-300	-/X	-/T	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1207-1208	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	956-957	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1029-1030	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	896-897	537-538	179-180	-/X	-/T	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1150-1151	897-898	299-300	-/X	-/T	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1204-1205	897-898	299-300	-/X	-/T	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1280-1281	-	-	-	-	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634676	17:7670694-7670694	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1157-1158	897-898	299-300	-/X	-/T	rs1567542146,COSV104584845,COSV52669776,COSV52691801	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1152-1153	1010-1011	337	R/X	cGC/c	rs1131691040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1276-1277	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1146-1147	1010-1011	337	R/X	cGC/c	rs1131691040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1203-1204	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4530;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	952-953	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	892-893	614-615	205	R/X	cGC/c	rs1131691040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3827;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4417;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2836;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1025-1026	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3518;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4463;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1260-1261	893-894	298	R/X	cGC/c	rs1131691040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1203-1204	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	952-953	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1025-1026	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	892-893	533-534	178	R/X	cGC/c	rs1131691040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1146-1147	893-894	298	R/X	cGC/c	rs1131691040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1200-1201	893-894	298	R/X	cGC/c	rs1131691040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1276-1277	-	-	-	-	rs1131691040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
428906	17:7670697-7670699	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1153-1154	893-894	298	R/X	cGC/c	rs1131691040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1145	?-1003	?-335	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567542245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567542245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,3_prime_UTR_variant,intron_variant	?-1269	-	-	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1139	?-1003	?-335	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,3_prime_UTR_variant,intron_variant	?-1196	-	-	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4492;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,3_prime_UTR_variant,intron_variant	?-945	-	-	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-885	?-607	?-203	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3789;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4379;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2798;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,3_prime_UTR_variant,intron_variant	?-1018	-	-	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3480;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3517;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1567542245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4425;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1253	?-886	?-296	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,3_prime_UTR_variant,intron_variant	?-1196	-	-	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,3_prime_UTR_variant,intron_variant	?-945	-	-	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,3_prime_UTR_variant,intron_variant	?-1018	-	-	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-885	?-526	?-176	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1139	?-886	?-296	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1193	?-886	?-296	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,3_prime_UTR_variant,intron_variant	?-1269	-	-	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634780	17:7670705-7670737	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant,NMD_transcript_variant	?-1146	?-886	?-296	-	-	rs1567542245	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1142	1000	334	G/W	Ggg/Tgg	rs730882028,CM134054,COSV52820679	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1266	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1136	1000	334	G/W	Ggg/Tgg	rs730882028,CM134054,COSV52820679	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1193	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4520;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	942	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	882	604	202	G/W	Ggg/Tgg	rs730882028,CM134054,COSV52820679	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3817;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4407;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2826;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1015	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3508;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4453;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1250	883	295	G/W	Ggg/Tgg	rs730882028,CM134054,COSV52820679	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1193	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	942	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1015	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	882	523	175	G/W	Ggg/Tgg	rs730882028,CM134054,COSV52820679	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1136	883	295	G/W	Ggg/Tgg	rs730882028,CM134054,COSV52820679	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1190	883	295	G/W	Ggg/Tgg	rs730882028,CM134054,COSV52820679	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1266	-	-	-	-	rs730882028,CM134054,COSV52820679	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428876	17:7670709-7670709	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1143	883	295	G/W	Ggg/Tgg	rs730882028,CM134054,COSV52820679	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant,splice_region_variant	1138-1139	996-997	332-333	IR/MX	atCCgt/atgt	rs1567542299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567542299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567542299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,3_prime_UTR_variant	1262-1263	-	-	-	-	rs1567542299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant,splice_region_variant	1132-1133	996-997	332-333	IR/MX	atCCgt/atgt	rs1567542299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,3_prime_UTR_variant	1189-1190	-	-	-	-	rs1567542299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4516;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,3_prime_UTR_variant	938-939	-	-	-	-	rs1567542299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant,splice_region_variant	878-879	600-601	200-201	IR/MX	atCCgt/atgt	rs1567542299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3813;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4403;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2822;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,3_prime_UTR_variant	1011-1012	-	-	-	-	rs1567542299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3504;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3541;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1567542299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567542299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4449;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant,splice_region_variant	1246-1247	879-880	293-294	IR/MX	atCCgt/atgt	rs1567542299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,3_prime_UTR_variant	1189-1190	-	-	-	-	rs1567542299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,3_prime_UTR_variant	938-939	-	-	-	-	rs1567542299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,3_prime_UTR_variant	1011-1012	-	-	-	-	rs1567542299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant,splice_region_variant	878-879	519-520	173-174	IR/MX	atCCgt/atgt	rs1567542299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant,splice_region_variant	1132-1133	879-880	293-294	IR/MX	atCCgt/atgt	rs1567542299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant,splice_region_variant	1186-1187	879-880	293-294	IR/MX	atCCgt/atgt	rs1567542299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,3_prime_UTR_variant	1262-1263	-	-	-	-	rs1567542299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634781	17:7670711-7670713	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,splice_region_variant,NMD_transcript_variant	1139-1140	879-880	293-294	IR/MX	atCCgt/atgt	rs1567542299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant,splice_region_variant	1137	995	332	I/N	aTc/aAc	COSV105872852,COSV53123312	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV105872852,COSV53123312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV105872852,COSV53123312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,3_prime_UTR_variant	1261	-	-	-	-	COSV105872852,COSV53123312	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant,splice_region_variant	1131	995	332	I/N	aTc/aAc	COSV105872852,COSV53123312	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,3_prime_UTR_variant	1188	-	-	-	-	COSV105872852,COSV53123312	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105872852,COSV53123312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4515;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,3_prime_UTR_variant	937	-	-	-	-	COSV105872852,COSV53123312	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant,splice_region_variant	877	599	200	I/N	aTc/aAc	COSV105872852,COSV53123312	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105872852,COSV53123312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3812;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105872852,COSV53123312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4402;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105872852,COSV53123312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2821;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,3_prime_UTR_variant	1010	-	-	-	-	COSV105872852,COSV53123312	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105872852,COSV53123312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3503;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105872852,COSV53123312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	COSV105872852,COSV53123312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105872852,COSV53123312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4448;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant,splice_region_variant	1245	878	293	I/N	aTc/aAc	COSV105872852,COSV53123312	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,3_prime_UTR_variant	1188	-	-	-	-	COSV105872852,COSV53123312	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,3_prime_UTR_variant	937	-	-	-	-	COSV105872852,COSV53123312	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,3_prime_UTR_variant	1010	-	-	-	-	COSV105872852,COSV53123312	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant,splice_region_variant	877	518	173	I/N	aTc/aAc	COSV105872852,COSV53123312	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant,splice_region_variant	1131	878	293	I/N	aTc/aAc	COSV105872852,COSV53123312	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant,splice_region_variant	1185	878	293	I/N	aTc/aAc	COSV105872852,COSV53123312	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,3_prime_UTR_variant	1261	-	-	-	-	COSV105872852,COSV53123312	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1768732	17:7670714-7670714	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,splice_region_variant,NMD_transcript_variant	1138	878	293	I/N	aTc/aAc	COSV105872852,COSV53123312	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4513;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3810;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4400;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2819;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3501;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3538;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4446;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
142161	17:7670716-7670716	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4513;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3810;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4400;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2819;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3501;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3538;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4446;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
232659	17:7670716-7670716	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs587782272,CS002470,CS033842,CS103209,COSV52668116,COSV52746625,COSV52766192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4512;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3809;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4399;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2818;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3500;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4445;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
487000	17:7670717-7670717	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs867389695,CS159286,COSV52692098,COSV52692518,COSV53122371	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1134-?	992-?	331-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	992-?	992-?	331-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1125-?	992-?	331-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1128-?	992-?	331-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1125-?	992-?	331-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1693;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	874-?	596-?	199-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	874-?	596-?	199-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1580;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000509690.5	Transcript	coding_sequence_variant,3_prime_UTR_variant	728-?	596-?	199-?	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	874-?	596-?	199-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=681;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000576024.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	52-?	53-?	18-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1626;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1242-?	875-?	292-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1125-?	875-?	292-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	874-?	515-?	172-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	874-?	515-?	172-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	874-?	515-?	172-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1128-?	875-?	292-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1182-?	875-?	292-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1125-?	875-?	292-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant,NMD_transcript_variant	1135-?	875-?	292-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1490777	17:7673527-7673536	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
1490777	17:7673527-7673536	-	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=TF_binding_site
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1695;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=992;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1582;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000576024.1	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1628;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428898	17:7673533-7673534	-	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1131691033,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1696;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=993;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1583;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=684;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=721;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000576024.1	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1629;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
635384	17:7673533-7673533	C	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597359053,COSV52703680,COSV52798259,COSV52814192	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1695;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=992;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1582;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000576024.1	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1628;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
379801	17:7673534-7673534	G	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant,splice_region_variant	1132-1135	990-993	330-331	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant,splice_region_variant	990-993	990-993	330-331	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant,splice_region_variant	1123-1126	990-993	330-331	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant,splice_region_variant	1126-1129	990-993	330-331	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant,splice_region_variant	1123-1126	990-993	330-331	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1691;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant,splice_region_variant	872-875	594-597	198-199	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant,splice_region_variant	872-875	594-597	198-199	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=988;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1578;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	726-729	594-597	198-199	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant,splice_region_variant	872-875	594-597	198-199	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=679;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=716;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant,splice_region_variant	50-53	51-54	17-18	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1624;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant,splice_region_variant	1240-1243	873-876	291-292	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant,splice_region_variant	1123-1126	873-876	291-292	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant,splice_region_variant	872-875	513-516	171-172	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant,splice_region_variant	872-875	513-516	171-172	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant,splice_region_variant	872-875	513-516	171-172	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant,splice_region_variant	1126-1129	873-876	291-292	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant,splice_region_variant	1180-1183	873-876	291-292	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant,splice_region_variant	1123-1126	873-876	291-292	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,splice_region_variant,NMD_transcript_variant	1133-1136	873-876	291-292	LQ/X	ctTCAG/ct	rs1555524949	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555524949	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
458579	17:7673534-7673538	-	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555524949	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=pathogenic;PHENO=1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1695;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=992;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1582;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000576024.1	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1628;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
528261	17:7673534-7673534	T	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1695;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=992;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1582;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000576024.1	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1628;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634766	17:7673534-7673534	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs11575997,CD002536,CS169329,COSV52663229,COSV52699909,COSV52752826	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant,splice_region_variant	1134-1135	992-993	331	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant,splice_region_variant	992-993	992-993	331	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV99467928	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant,splice_region_variant	1125-1126	992-993	331	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant,splice_region_variant	1128-1129	992-993	331	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant,splice_region_variant	1125-1126	992-993	331	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99467928	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1693;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant,splice_region_variant	874-875	596-597	199	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant,splice_region_variant	874-875	596-597	199	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99467928	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99467928	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1580;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	728-729	596-597	199	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant,splice_region_variant	874-875	596-597	199	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99467928	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=681;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99467928	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant,splice_region_variant	52-53	53-54	18	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99467928	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1626;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant,splice_region_variant	1242-1243	875-876	292	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant,splice_region_variant	1125-1126	875-876	292	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant,splice_region_variant	874-875	515-516	172	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant,splice_region_variant	874-875	515-516	172	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant,splice_region_variant	874-875	515-516	172	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant,splice_region_variant	1128-1129	875-876	292	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant,splice_region_variant	1182-1183	875-876	292	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant,splice_region_variant	1125-1126	875-876	292	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,splice_region_variant,NMD_transcript_variant	1135-1136	875-876	292	Q/QPAPLPSQRRNHWMENISPFX	cag/caACCAGCTCCTCTCCCCAGCCAAAGAAGAAACCACTGGATGGAGAATATTTCACCCTTCAg	COSV99467928	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV99467928	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1;PHENO=1
1066203	17:7673535-7673535	TGAAGGGTGAAATATTCTCCATCCAGTGGTTTCTTCTTTGGCTGGGGAGAGGAGCTGGT	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV99467928	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;SOMATIC=1;PHENO=1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	1135	993	331	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,synonymous_variant	993	993	331	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,synonymous_variant	1126	993	331	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	1129	993	331	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,synonymous_variant	1126	993	331	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1694;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,synonymous_variant	875	597	199	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,synonymous_variant	875	597	199	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=991;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1581;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	729	597	199	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,synonymous_variant	875	597	199	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=682;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=719;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000576024.1	Transcript	splice_region_variant,synonymous_variant	53	54	18	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1627;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,synonymous_variant	1243	876	292	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,synonymous_variant	1126	876	292	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,synonymous_variant	875	516	172	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,synonymous_variant	875	516	172	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,synonymous_variant	875	516	172	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,synonymous_variant	1129	876	292	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,synonymous_variant	1183	876	292	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,synonymous_variant	1126	876	292	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,synonymous_variant,NMD_transcript_variant	1136	876	292	Q	caG/caA	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428868	17:7673535-7673535	T	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs11575996,CS125161,COSV52681350,COSV52690011,COSV52951377,COSV99391417	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1132	990	330	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	990	990	330	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1123	990	330	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1126	990	330	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1123	990	330	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1691;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	872	594	198	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	872	594	198	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=988;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1578;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	726	594	198	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	872	594	198	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=679;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=716;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	50	51	17	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1624;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1240	873	291	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1123	873	291	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	872	513	171	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	872	513	171	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	872	513	171	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1126	873	291	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1180	873	291	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1123	873	291	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1133	873	291	L/X	ctT/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1378020	17:7673537-7673538	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
1378020	17:7673537-7673538	-	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=TF_binding_site
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained,splice_region_variant	1133	991	331	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained,splice_region_variant	991	991	331	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	CM1511153,COSV52664188	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained,splice_region_variant	1124	991	331	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained,splice_region_variant	1127	991	331	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained,splice_region_variant	1124	991	331	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM1511153,COSV52664188	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1692;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained,splice_region_variant	873	595	199	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained,splice_region_variant	873	595	199	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM1511153,COSV52664188	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=989;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM1511153,COSV52664188	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1579;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	727	595	199	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained,splice_region_variant	873	595	199	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM1511153,COSV52664188	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=680;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM1511153,COSV52664188	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000576024.1	Transcript	stop_gained,splice_region_variant	51	52	18	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM1511153,COSV52664188	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1625;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained,splice_region_variant	1241	874	292	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained,splice_region_variant	1124	874	292	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained,splice_region_variant	873	514	172	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained,splice_region_variant	873	514	172	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained,splice_region_variant	873	514	172	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained,splice_region_variant	1127	874	292	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained,splice_region_variant	1181	874	292	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained,splice_region_variant	1124	874	292	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,splice_region_variant,NMD_transcript_variant	1134	874	292	Q/*	Cag/Tag	CM1511153,COSV52664188	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	CM1511153,COSV52664188	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,1;PHENO=1,1
922893	17:7673537-7673537	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	CM1511153,COSV52664188	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;SOMATIC=0,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1130	988	330	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	988	988	330	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV53825922,COSV99461761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1121	988	330	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1124	988	330	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1121	988	330	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53825922,COSV99461761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1689;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	870	592	198	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	870	592	198	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53825922,COSV99461761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=986;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53825922,COSV99461761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1576;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	724	592	198	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	870	592	198	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53825922,COSV99461761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=677;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53825922,COSV99461761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=714;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	48	49	17	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53825922,COSV99461761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1622;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1238	871	291	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1121	871	291	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	870	511	171	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	870	511	171	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	870	511	171	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1124	871	291	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1178	871	291	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1121	871	291	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1131	871	291	L/X	Ctt/tt	COSV53825922,COSV99461761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV53825922,COSV99461761	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1;PHENO=1,1
952204	17:7673539-7673540	-	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV53825922,COSV99461761	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;SOMATIC=1,1;PHENO=1,1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1110-1128	968-986	323-329	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	968-986	968-986	323-329	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567545918	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1101-1119	968-986	323-329	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1104-1122	968-986	323-329	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1101-1119	968-986	323-329	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545918	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1669;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	850-868	572-590	191-197	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	850-868	572-590	191-197	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545918	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=966;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545918	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1556;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	704-722	572-590	191-197	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	850-868	572-590	191-197	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545918	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=657;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545918	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=694;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	28-46	29-47	10-16	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545918	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1602;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1218-1236	851-869	284-290	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1101-1119	851-869	284-290	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	850-868	491-509	164-170	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	850-868	491-509	164-170	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	850-868	491-509	164-170	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1104-1122	851-869	284-290	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1158-1176	851-869	284-290	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1101-1119	851-869	284-290	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1111-1129	851-869	284-290	LDGEYFT/X	cTGGATGGAGAATATTTCACc/cc	rs1567545918	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567545918	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
628459	17:7673541-7673560	-	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567545918	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=pathogenic;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1125-1126	983-984	328	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	983-984	983-984	328	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1116-1117	983-984	328	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1119-1120	983-984	328	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1116-1117	983-984	328	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1684;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	865-866	587-588	196	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	865-866	587-588	196	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=981;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1571;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	719-720	587-588	196	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	865-866	587-588	196	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=672;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=709;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	43-44	44-45	15	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1617;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1233-1234	866-867	289	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1116-1117	866-867	289	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	865-866	506-507	169	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	865-866	506-507	169	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	865-866	506-507	169	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1119-1120	866-867	289	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1173-1174	866-867	289	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1116-1117	866-867	289	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1126-1127	866-867	289	F/FX	ttc/ttTTc	COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52927593	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1;PHENO=1
1456557	17:7673544-7673544	AA	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52927593	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;SOMATIC=1;PHENO=1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1125-1126	983-984	328	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	983-984	983-984	328	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs886041285,COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1116-1117	983-984	328	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1119-1120	983-984	328	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1116-1117	983-984	328	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs886041285,COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1684;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	865-866	587-588	196	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	865-866	587-588	196	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886041285,COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=981;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886041285,COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1571;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	719-720	587-588	196	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	865-866	587-588	196	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886041285,COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=672;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs886041285,COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=709;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	43-44	44-45	15	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886041285,COSV52927593	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1617;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1233-1234	866-867	289	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1116-1117	866-867	289	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	865-866	506-507	169	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	865-866	506-507	169	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	865-866	506-507	169	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1119-1120	866-867	289	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1173-1174	866-867	289	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1116-1117	866-867	289	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1126-1127	866-867	289	F/FX	ttc/ttTc	rs886041285,COSV52927593	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs886041285,COSV52927593	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
279962	17:7673544-7673544	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs886041285,COSV52927593	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1122-1123	980-981	327	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	980-981	980-981	327	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597359215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1113-1114	980-981	327	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1116-1117	980-981	327	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1113-1114	980-981	327	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1681;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	862-863	584-585	195	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	862-863	584-585	195	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=978;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1568;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	716-717	584-585	195	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	862-863	584-585	195	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=669;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=706;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	40-41	41-42	14	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1614;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1230-1231	863-864	288	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1113-1114	863-864	288	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	862-863	503-504	168	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	862-863	503-504	168	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	862-863	503-504	168	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1116-1117	863-864	288	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1170-1171	863-864	288	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1113-1114	863-864	288	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1123-1124	863-864	288	Y/X	tAT/t	rs1597359215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634783	17:7673546-7673548	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597359215	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;PHENO=1
634783	17:7673546-7673548	-	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597359215	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;PHENO=1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1123	981	327	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	981	981	327	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	1114	981	327	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1117	981	327	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	1114	981	327	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1682;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	863	585	195	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	863	585	195	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=979;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1569;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	717	585	195	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	863	585	195	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=670;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=707;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000576024.1	Transcript	stop_gained	41	42	14	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1615;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1231	864	288	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	1114	864	288	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	863	504	168	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	863	504	168	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	863	504	168	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1117	864	288	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1171	864	288	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	1114	864	288	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1124	864	288	Y/*	taT/taA	COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1,1;PHENO=1,1,1
1361331	17:7673547-7673547	T	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;SOMATIC=1,1,1;PHENO=1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1123	981	327	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	981	981	327	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	1114	981	327	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1117	981	327	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	1114	981	327	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1682;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	863	585	195	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	863	585	195	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=979;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1569;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	717	585	195	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	863	585	195	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=670;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=707;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000576024.1	Transcript	stop_gained	41	42	14	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1615;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1231	864	288	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	1114	864	288	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	863	504	168	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	863	504	168	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	863	504	168	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1117	864	288	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1171	864	288	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	1114	864	288	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1124	864	288	Y/*	taT/taG	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
246069	17:7673547-7673547	C	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs879254077,COSV52678878,COSV52914365,COSV52993701	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1119-1120	977-978	326	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	977-978	977-978	326	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597359235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1110-1111	977-978	326	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1113-1114	977-978	326	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1110-1111	977-978	326	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1678;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	859-860	581-582	194	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	859-860	581-582	194	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=975;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1565;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	713-714	581-582	194	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	859-860	581-582	194	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=703;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	37-38	38-39	13	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1611;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1227-1228	860-861	287	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1110-1111	860-861	287	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	859-860	500-501	167	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	859-860	500-501	167	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	859-860	500-501	167	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1113-1114	860-861	287	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1167-1168	860-861	287	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1110-1111	860-861	287	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1120-1121	860-861	287	E/EX	gaa/gaGAa	rs1597359235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
823466	17:7673550-7673550	TC	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597359235	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;PHENO=1
823466	17:7673550-7673550	TC	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597359235	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;PHENO=1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1118	976	326	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	976	976	326	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	1109	976	326	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1112	976	326	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	1109	976	326	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1677;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	858	580	194	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	858	580	194	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=974;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1564;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	712	580	194	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	858	580	194	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=665;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=702;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000576024.1	Transcript	stop_gained	36	37	13	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1610;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1226	859	287	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	1109	859	287	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	858	499	167	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	858	499	167	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	858	499	167	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1112	859	287	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1166	859	287	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	1109	859	287	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1119	859	287	E/*	Gaa/Taa	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231815	17:7673552-7673552	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs876659384,COSV105017877,COSV52700095,COSV52863161	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1115	973	325	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	973	973	325	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs863224500,COSV52982163,COSV53644278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	1106	973	325	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1109	973	325	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	1106	973	325	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224500,COSV52982163,COSV53644278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1674;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	855	577	193	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	855	577	193	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224500,COSV52982163,COSV53644278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224500,COSV52982163,COSV53644278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1561;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	709	577	193	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	855	577	193	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224500,COSV52982163,COSV53644278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=662;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224500,COSV52982163,COSV53644278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=699;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000576024.1	Transcript	stop_gained	33	34	12	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224500,COSV52982163,COSV53644278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1607;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1223	856	286	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	1106	856	286	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	855	496	166	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	855	496	166	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	855	496	166	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1109	856	286	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1163	856	286	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	1106	856	286	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1116	856	286	G/*	Gga/Tga	rs863224500,COSV52982163,COSV53644278	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs863224500,COSV52982163,COSV53644278	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
216079	17:7673555-7673555	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs863224500,COSV52982163,COSV53644278	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1112	970	324	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	970	970	324	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524970,CM161003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1103	970	324	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1106	970	324	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1103	970	324	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524970,CM161003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1671;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	852	574	192	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	852	574	192	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524970,CM161003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=968;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524970,CM161003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1558;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	706	574	192	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	852	574	192	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524970,CM161003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524970,CM161003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	30	31	11	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524970,CM161003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1604;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1220	853	285	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1103	853	285	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	852	493	165	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	852	493	165	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	852	493	165	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1106	853	285	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1160	853	285	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1103	853	285	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1113	853	285	D/X	Gat/at	rs1555524970,CM161003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555524970,CM161003	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic;PHENO=1,1
492744	17:7673557-7673558	-	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555524970,CM161003	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_pathogenic;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1107	965	322	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	965	965	322	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52729459,COSV52826955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1098	965	322	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1101	965	322	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1098	965	322	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52729459,COSV52826955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1666;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	847	569	190	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	847	569	190	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52729459,COSV52826955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=963;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52729459,COSV52826955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1553;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	701	569	190	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	847	569	190	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52729459,COSV52826955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=654;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52729459,COSV52826955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=691;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	25	26	9	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52729459,COSV52826955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1599;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1215	848	283	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1098	848	283	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	847	488	163	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	847	488	163	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	847	488	163	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1101	848	283	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1155	848	283	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1098	848	283	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1108	848	283	P/X	cCa/ca	COSV52729459,COSV52826955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52729459,COSV52826955	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1;PHENO=1,1
1767691	17:7673562-7673563	-	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52729459,COSV52826955	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;SOMATIC=1,1;PHENO=1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1103	961	321	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	961	961	321	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2073154382,COSV52686338,COSV52850306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	1094	961	321	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1097	961	321	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	1094	961	321	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073154382,COSV52686338,COSV52850306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1662;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	843	565	189	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	843	565	189	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073154382,COSV52686338,COSV52850306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=959;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073154382,COSV52686338,COSV52850306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1549;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	697	565	189	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	843	565	189	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073154382,COSV52686338,COSV52850306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=650;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073154382,COSV52686338,COSV52850306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=687;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000576024.1	Transcript	stop_gained	21	22	8	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073154382,COSV52686338,COSV52850306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1595;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1211	844	282	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	1094	844	282	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	843	484	162	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	843	484	162	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	843	484	162	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1097	844	282	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1151	844	282	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	1094	844	282	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1104	844	282	K/*	Aaa/Taa	rs2073154382,COSV52686338,COSV52850306	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2073154382,COSV52686338,COSV52850306	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
842397	17:7673567-7673567	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2073154382,COSV52686338,COSV52850306	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1100	958	320	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	958	958	320	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52972883,COSV53297326,COSV99398075	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	1091	958	320	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1094	958	320	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	1091	958	320	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52972883,COSV53297326,COSV99398075	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1659;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	840	562	188	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	840	562	188	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52972883,COSV53297326,COSV99398075	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=956;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52972883,COSV53297326,COSV99398075	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1546;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	694	562	188	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	840	562	188	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52972883,COSV53297326,COSV99398075	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=647;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52972883,COSV53297326,COSV99398075	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=684;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000576024.1	Transcript	stop_gained	18	19	7	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52972883,COSV53297326,COSV99398075	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1592;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1208	841	281	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	1091	841	281	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	840	481	161	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	840	481	161	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	840	481	161	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1094	841	281	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1148	841	281	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	1091	841	281	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1101	841	281	K/*	Aag/Tag	COSV52972883,COSV53297326,COSV99398075	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1075711	17:7673570-7673570	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52972883,COSV53297326,COSV99398075	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1,1;PHENO=1,1,1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1093-1096	951-954	317-318	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	951-954	951-954	317-318	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597359403	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1084-1087	951-954	317-318	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1087-1090	951-954	317-318	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1084-1087	951-954	317-318	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359403	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1652;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	833-836	555-558	185-186	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	833-836	555-558	185-186	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359403	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=949;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359403	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1539;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	687-690	555-558	185-186	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	833-836	555-558	185-186	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359403	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=640;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359403	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=677;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	11-14	12-15	4-5	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359403	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1585;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1201-1204	834-837	278-279	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1084-1087	834-837	278-279	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	833-836	474-477	158-159	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	833-836	474-477	158-159	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	833-836	474-477	158-159	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1087-1090	834-837	278-279	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1141-1144	834-837	278-279	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1084-1087	834-837	278-279	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1094-1097	834-837	278-279	QP/X	caGCCA/ca	rs1597359403	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823302	17:7673573-7673577	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597359403	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1092	950	317	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	950	950	317	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1083	950	317	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1086	950	317	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1083	950	317	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1651;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	832	554	185	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	832	554	185	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=948;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1538;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	686	554	185	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	832	554	185	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=676;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	10	11	4	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1584;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1200	833	278	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1083	833	278	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	832	473	158	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	832	473	158	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	832	473	158	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1086	833	278	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1140	833	278	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1083	833	278	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1093	833	278	Q/X	cAg/cg	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480747	17:7673577-7673578	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555524976,COSV52666793,COSV53038648,COSV53135590	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1091	949	317	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	949	949	317	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567546196,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1082	949	317	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1085	949	317	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1082	949	317	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546196,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1650;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	831	553	185	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	831	553	185	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546196,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=947;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546196,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1537;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	685	553	185	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	831	553	185	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546196,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=638;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546196,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=675;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	9	10	4	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546196,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1583;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1199	832	278	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1082	832	278	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	831	472	158	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	831	472	158	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	831	472	158	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1085	832	278	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1139	832	278	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1082	832	278	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1092	832	278	Q/X	Cag/ag	rs1567546196,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
577286	17:7673578-7673579	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567546196,COSV52685086,COSV53209009	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1091	949	317	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	949	949	317	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	1082	949	317	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1085	949	317	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	1082	949	317	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1650;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	831	553	185	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	831	553	185	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=947;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1537;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	685	553	185	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	831	553	185	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=638;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=675;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000576024.1	Transcript	stop_gained	9	10	4	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1583;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1199	832	278	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	1082	832	278	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	831	472	158	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	831	472	158	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	831	472	158	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1085	832	278	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1139	832	278	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	1082	832	278	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1092	832	278	Q/*	Cag/Tag	rs764735889,COSV52685086,COSV53209009	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
450344	17:7673579-7673579	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1087-1088	945-946	315-316	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	945-946	945-946	315-316	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1078-1079	945-946	315-316	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1081-1082	945-946	315-316	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1078-1079	945-946	315-316	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1646;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	827-828	549-550	183-184	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	827-828	549-550	183-184	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=943;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1533;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	681-682	549-550	183-184	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	827-828	549-550	183-184	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=634;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=671;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	5-6	6-7	2-3	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1579;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1195-1196	828-829	276-277	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1078-1079	828-829	276-277	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	827-828	468-469	156-157	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	827-828	468-469	156-157	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	827-828	468-469	156-157	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1081-1082	828-829	276-277	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1135-1136	828-829	276-277	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1078-1079	828-829	276-277	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1088-1089	828-829	276-277	SP/SX	tcTCcc/tccc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1391019	17:7673581-7673583	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1079-1088	937-946	313-316	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	937-946	937-946	313-316	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567546226	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1070-1079	937-946	313-316	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1073-1082	937-946	313-316	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1070-1079	937-946	313-316	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546226	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1638;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	819-828	541-550	181-184	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	819-828	541-550	181-184	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546226	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=935;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546226	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1525;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	673-682	541-550	181-184	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	819-828	541-550	181-184	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546226	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546226	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=663;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000576024.1	Transcript	coding_sequence_variant,5_prime_UTR_variant	?-6	?-7	?-3	-	-	rs1567546226	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546226	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1571;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1187-1196	820-829	274-277	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1070-1079	820-829	274-277	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	819-828	460-469	154-157	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	819-828	460-469	154-157	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	819-828	460-469	154-157	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1073-1082	820-829	274-277	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1127-1136	820-829	274-277	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1070-1079	820-829	274-277	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1080-1089	820-829	274-277	SSSP/X	AGCTCCTCTCcc/cc	rs1567546226	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634767	17:7673581-7673591	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567546226	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1087-1088	945-946	315-316	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	945-946	945-946	315-316	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52867051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1078-1079	945-946	315-316	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1081-1082	945-946	315-316	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1078-1079	945-946	315-316	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52867051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1646;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	827-828	549-550	183-184	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	827-828	549-550	183-184	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52867051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=943;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52867051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1533;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	681-682	549-550	183-184	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	827-828	549-550	183-184	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52867051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=634;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52867051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=671;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	5-6	6-7	2-3	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52867051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1579;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1195-1196	828-829	276-277	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1078-1079	828-829	276-277	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	827-828	468-469	156-157	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	827-828	468-469	156-157	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	827-828	468-469	156-157	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1081-1082	828-829	276-277	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1135-1136	828-829	276-277	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1078-1079	828-829	276-277	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1088-1089	828-829	276-277	-/X	-/T	COSV52867051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1425093	17:7673582-7673582	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52867051	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1;PHENO=1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1087	945	315	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	945	945	315	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597359548,COSV53686305,COSV53835235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1078	945	315	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1081	945	315	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1078	945	315	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359548,COSV53686305,COSV53835235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1646;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	827	549	183	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	827	549	183	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359548,COSV53686305,COSV53835235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=943;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359548,COSV53686305,COSV53835235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1533;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	681	549	183	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	827	549	183	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359548,COSV53686305,COSV53835235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=634;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359548,COSV53686305,COSV53835235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=671;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000576024.1	Transcript	frameshift_variant	5	6	2	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359548,COSV53686305,COSV53835235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1579;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1195	828	276	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1078	828	276	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	827	468	156	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	827	468	156	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	827	468	156	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1081	828	276	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1135	828	276	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1078	828	276	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1088	828	276	S/X	tcT/tc	rs1597359548,COSV53686305,COSV53835235	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
663914	17:7673582-7673583	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597359548,COSV53686305,COSV53835235	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1075	933	311	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	933	933	311	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567546373,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1066	933	311	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1069	933	311	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1066	933	311	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546373,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1634;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	815	537	179	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	815	537	179	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546373,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=931;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546373,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1521;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	669	537	179	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	815	537	179	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546373,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=622;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546373,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567546373,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=8;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546373,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1567;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1183	816	272	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1066	816	272	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	815	456	152	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	815	456	152	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	815	456	152	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1069	816	272	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1123	816	272	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1066	816	272	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1076	816	272	N/X	aaC/aa	rs1567546373,COSV53154719,COSV53486992	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634787	17:7673594-7673595	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567546373,COSV53154719,COSV53486992	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1074-1075	932-933	311	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	932-933	932-933	311	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1065-1066	932-933	311	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1068-1069	932-933	311	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1065-1066	932-933	311	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1633;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	814-815	536-537	179	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	814-815	536-537	179	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=930;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1520;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	668-669	536-537	179	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	814-815	536-537	179	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=658;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=8;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1566;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1182-1183	815-816	272	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1065-1066	815-816	272	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	814-815	455-456	152	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	814-815	455-456	152	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	814-815	455-456	152	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1068-1069	815-816	272	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1122-1123	815-816	272	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1065-1066	815-816	272	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1075-1076	815-816	272	N/KX	aac/aaAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766586	17:7673595-7673595	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1069	927	309	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	927	927	309	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1060	927	309	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1063	927	309	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1060	927	309	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1628;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	809	531	177	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	809	531	177	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=925;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1515;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	663	531	177	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	809	531	177	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=616;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=653;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1561;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1177	810	270	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1060	810	270	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	809	450	150	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	809	450	150	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	809	450	150	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1063	810	270	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1117	810	270	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1060	810	270	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1070	810	270	P/X	ccC/cc	COSV53371983	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
871292	17:7673600-7673601	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV53371983	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1;PHENO=1
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1062	?-920	?-307	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-920	?-920	?-307	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1053	?-920	?-307	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1056	?-920	?-307	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1053	?-920	?-307	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1617;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-802	?-524	?-175	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-802	?-524	?-175	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=914;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1504;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-656	?-524	?-175	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-802	?-524	?-175	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=605;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=642;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=21;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1550;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1170	?-803	?-268	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1053	?-803	?-268	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-802	?-443	?-148	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-802	?-443	?-148	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-802	?-443	?-148	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1056	?-803	?-268	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1110	?-803	?-268	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1053	?-803	?-268	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant,NMD_transcript_variant	?-1063	?-803	?-268	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1486334	17:7673607-7673612	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1620;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=917;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1507;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=608;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=645;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=22;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1553;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
141377	17:7673609-7673609	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1620;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=917;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1507;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=608;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=645;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=22;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1553;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406610	17:7673609-7673609	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1620;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=917;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1507;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=608;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=645;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=22;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1553;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
480765	17:7673609-7673609	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs587781702,CS0910927,CS114009,COSV52664150,COSV52690279,COSV52737535	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1619;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=916;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1506;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=607;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=644;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=23;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1552;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
43595	17:7673610-7673610	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs397516439,COSV52693974,COSV52706655,COSV52945558,COSV53066011	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1059-?	917-?	306-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	917-?	917-?	306-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597360140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1050-?	917-?	306-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1053-?	917-?	306-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1050-?	917-?	306-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1526;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	521-?	174-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	521-?	174-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=823;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1413;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	653-?	521-?	174-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	521-?	174-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=514;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=551;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597360140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=99;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1459;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1167-?	800-?	267-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1050-?	800-?	267-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	440-?	147-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	440-?	147-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	440-?	147-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1053-?	800-?	267-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1107-?	800-?	267-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1050-?	800-?	267-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant,NMD_transcript_variant	1060-?	800-?	267-?	-	-	rs1597360140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
660287	17:7673685-7673703	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597360140	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1059-?	917-?	306-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	917-?	917-?	306-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1050-?	917-?	306-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1053-?	917-?	306-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1050-?	917-?	306-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1526;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	521-?	174-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	521-?	174-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=823;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1413;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	653-?	521-?	174-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	521-?	174-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=514;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=551;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=104;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1459;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1167-?	800-?	267-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1050-?	800-?	267-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	440-?	147-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	440-?	147-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	440-?	147-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1053-?	800-?	267-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1107-?	800-?	267-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1050-?	800-?	267-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant,NMD_transcript_variant	1060-?	800-?	267-?	-	-	rs1555525040	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528253	17:7673690-7673703	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525040	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1059-?	917-?	306-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	917-?	917-?	306-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567546716	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1050-?	917-?	306-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1053-?	917-?	306-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1050-?	917-?	306-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546716	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1526;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	521-?	174-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	521-?	174-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546716	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=823;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546716	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1413;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	653-?	521-?	174-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	521-?	174-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546716	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=514;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546716	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=551;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567546716	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=108;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546716	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1459;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1167-?	800-?	267-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1050-?	800-?	267-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	440-?	147-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	440-?	147-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	799-?	440-?	147-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1053-?	800-?	267-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1107-?	800-?	267-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1050-?	800-?	267-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant,NMD_transcript_variant	1060-?	800-?	267-?	-	-	rs1567546716	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
570307	17:7673694-7673703	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567546716	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1529;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=826;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1416;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=517;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=554;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=113;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1462;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1068484	17:7673699-7673700	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1530;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=827;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1417;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=518;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=112;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1463;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428877	17:7673699-7673699	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1530;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=827;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1417;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=518;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=112;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1463;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
633608	17:7673699-7673699	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1131691016,COSV52698436,COSV52737448,COSV52774697	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1529;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=826;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1416;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=517;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=554;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=113;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1462;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
428905	17:7673700-7673700	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1529;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=826;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1416;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=517;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=554;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=113;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1462;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
495326	17:7673700-7673700	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1529;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=826;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1416;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=517;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=554;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=113;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1462;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
633606	17:7673700-7673700	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1131691039,CD920913,CS107068,CS120864,COSV52683145,COSV52775982,COSV52814989	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained,frameshift_variant,splice_region_variant	1061-1062	919-920	307	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained,frameshift_variant,splice_region_variant	919-920	919-920	307	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained,frameshift_variant,splice_region_variant	1052-1053	919-920	307	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained,frameshift_variant,splice_region_variant	1055-1056	919-920	307	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained,frameshift_variant,splice_region_variant	1052-1053	919-920	307	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1528;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained,frameshift_variant,splice_region_variant	801-802	523-524	175	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained,frameshift_variant,splice_region_variant	801-802	523-524	175	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=825;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1415;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained,frameshift_variant,splice_region_variant	655-656	523-524	175	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained,frameshift_variant,splice_region_variant	801-802	523-524	175	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=516;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=553;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=113;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1461;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained,frameshift_variant,splice_region_variant	1169-1170	802-803	268	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained,frameshift_variant,splice_region_variant	1052-1053	802-803	268	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained,frameshift_variant,splice_region_variant	801-802	442-443	148	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained,frameshift_variant,splice_region_variant	801-802	442-443	148	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained,frameshift_variant,splice_region_variant	801-802	442-443	148	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained,frameshift_variant,splice_region_variant	1055-1056	802-803	268	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained,frameshift_variant,splice_region_variant	1109-1110	802-803	268	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained,frameshift_variant,splice_region_variant	1052-1053	802-803	268	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,frameshift_variant,splice_region_variant,NMD_transcript_variant	1062-1063	802-803	268	A/AAPREH*ASX	gca/gCTGCCCCCAGGGAGCACTAAGCGAGca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
841830	17:7673700-7673700	CTCGCTTAGTGCTCCCTGGGGGCAG	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1058-1059	916-917	306	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	916-917	916-917	306	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597360326,COSV53301060	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1049-1050	916-917	306	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1052-1053	916-917	306	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1049-1050	916-917	306	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360326,COSV53301060	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1525;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	798-799	520-521	174	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	798-799	520-521	174	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360326,COSV53301060	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=822;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360326,COSV53301060	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1412;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	652-653	520-521	174	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	798-799	520-521	174	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360326,COSV53301060	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=513;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360326,COSV53301060	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597360326,COSV53301060	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=116;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360326,COSV53301060	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1458;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1166-1167	799-800	267	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1049-1050	799-800	267	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	798-799	439-440	147	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	798-799	439-440	147	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	798-799	439-440	147	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1052-1053	799-800	267	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1106-1107	799-800	267	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1049-1050	799-800	267	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1059-1060	799-800	267	R/PLSX	cga/cCACTAAGCga	rs1597360326,COSV53301060	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
823003	17:7673703-7673703	GCTTAGTG	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597360326,COSV53301060	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1058	916	306	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	916	916	306	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	1049	916	306	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1052	916	306	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	1049	916	306	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1525;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	798	520	174	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	798	520	174	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=822;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1412;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	652	520	174	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	798	520	174	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=513;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=117;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1458;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1166	799	267	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	1049	799	267	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	798	439	147	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	798	439	147	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	798	439	147	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1052	799	267	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1106	799	267	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	1049	799	267	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1059	799	267	R/*	Cga/Tga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
142144	17:7673704-7673704	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1054-1055	912-913	304-305	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	912-913	912-913	304-305	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567546818	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1045-1046	912-913	304-305	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1048-1049	912-913	304-305	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1045-1046	912-913	304-305	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546818	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1521;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	794-795	516-517	172-173	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	794-795	516-517	172-173	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546818	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=818;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546818	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1408;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	648-649	516-517	172-173	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	794-795	516-517	172-173	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546818	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=509;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546818	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567546818	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=120;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546818	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1454;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1162-1163	795-796	265-266	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1045-1046	795-796	265-266	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	794-795	435-436	145-146	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	794-795	435-436	145-146	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	794-795	435-436	145-146	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1048-1049	795-796	265-266	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1102-1103	795-796	265-266	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1045-1046	795-796	265-266	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1055-1056	795-796	265-266	-/X	-/T	rs1567546818	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
630788	17:7673707-7673707	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567546818	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1055	913	305	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	913	913	305	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597360340,COSV52688866,COSV52766207	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	1046	913	305	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1049	913	305	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	1046	913	305	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360340,COSV52688866,COSV52766207	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1522;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	795	517	173	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	795	517	173	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360340,COSV52688866,COSV52766207	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=819;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360340,COSV52688866,COSV52766207	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1409;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	649	517	173	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	795	517	173	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360340,COSV52688866,COSV52766207	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360340,COSV52688866,COSV52766207	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597360340,COSV52688866,COSV52766207	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=120;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360340,COSV52688866,COSV52766207	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1455;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1163	796	266	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	1046	796	266	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	795	436	146	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	795	436	146	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	795	436	146	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1049	796	266	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1103	796	266	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	1046	796	266	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1056	796	266	K/*	Aag/Tag	rs1597360340,COSV52688866,COSV52766207	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823045	17:7673707-7673707	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597360340,COSV52688866,COSV52766207	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1052-1053	910-911	304	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	910-911	910-911	304	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1043-1044	910-911	304	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1046-1047	910-911	304	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1043-1044	910-911	304	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1519;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	792-793	514-515	172	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	792-793	514-515	172	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=816;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1406;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	646-647	514-515	172	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	792-793	514-515	172	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=507;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=544;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=122;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1452;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1160-1161	793-794	265	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1043-1044	793-794	265	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	792-793	433-434	145	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	792-793	433-434	145	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	792-793	433-434	145	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1046-1047	793-794	265	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1100-1101	793-794	265	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1043-1044	793-794	265	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1053-1054	793-794	265	T/EVSKX	ACt/GAGGTAAGCAAGGt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965088	17:7673709-7673710	CCTTGCTTACCTC	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1038-1051	896-909	299-303	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	896-909	896-909	299-303	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525054	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1029-1042	896-909	299-303	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1032-1045	896-909	299-303	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1029-1042	896-909	299-303	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525054	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1505;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	778-791	500-513	167-171	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	778-791	500-513	167-171	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525054	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=802;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525054	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1392;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	632-645	500-513	167-171	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	778-791	500-513	167-171	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525054	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525054	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=530;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525054	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=124;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525054	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1438;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1146-1159	779-792	260-264	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1029-1042	779-792	260-264	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	778-791	419-432	140-144	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	778-791	419-432	140-144	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	778-791	419-432	140-144	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1032-1045	779-792	260-264	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1086-1099	779-792	260-264	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1029-1042	779-792	260-264	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1039-1052	779-792	260-264	LPPGS/X	cTGCCCCCAGGGAGC/c	rs1555525054	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492745	17:7673710-7673724	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525054	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1050-1051	908-909	303	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	908-909	908-909	303	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567546889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1041-1042	908-909	303	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1044-1045	908-909	303	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1041-1042	908-909	303	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1517;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	790-791	512-513	171	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	790-791	512-513	171	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=814;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1404;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	644-645	512-513	171	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	790-791	512-513	171	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=505;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=542;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567546889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=124;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567546889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1450;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1158-1159	791-792	264	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1041-1042	791-792	264	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	790-791	431-432	144	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	790-791	431-432	144	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	790-791	431-432	144	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1044-1045	791-792	264	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1098-1099	791-792	264	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1041-1042	791-792	264	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1051-1052	791-792	264	S/RGX	agc/agGGGGc	rs1567546889	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634782	17:7673711-7673711	CCCC	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567546889	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1048	906	302	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	906	906	302	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1039	906	302	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1042	906	302	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1039	906	302	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1515;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	788	510	170	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	788	510	170	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=812;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1402;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	642	510	170	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	788	510	170	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=503;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=127;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1448;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1156	789	263	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1039	789	263	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	788	429	143	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	788	429	143	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	788	429	143	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1042	789	263	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1096	789	263	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1039	789	263	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1049	789	263	G/X	ggG/gg	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185285	17:7673713-7673714	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs786202055,CD136786,COSV52761585,COSV52876415,COSV99037454	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1044-1045	902-903	301	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	902-903	902-903	301	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1035-1036	902-903	301	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1038-1039	902-903	301	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1035-1036	902-903	301	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1511;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	784-785	506-507	169	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	784-785	506-507	169	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=808;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1398;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	638-639	506-507	169	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	784-785	506-507	169	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=536;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=130;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1444;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1152-1153	785-786	262	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1035-1036	785-786	262	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	784-785	425-426	142	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	784-785	425-426	142	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	784-785	425-426	142	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1038-1039	785-786	262	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1092-1093	785-786	262	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1035-1036	785-786	262	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1045-1046	785-786	262	P/PX	cca/ccCa	COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1389237	17:7673717-7673717	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV53177081	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1;PHENO=1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1044	902	301	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	902	902	301	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs876660726,COSV53267099,COSV53486315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1035	902	301	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1038	902	301	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1035	902	301	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660726,COSV53267099,COSV53486315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1511;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	784	506	169	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	784	506	169	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660726,COSV53267099,COSV53486315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=808;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660726,COSV53267099,COSV53486315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1398;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	638	506	169	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	784	506	169	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660726,COSV53267099,COSV53486315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660726,COSV53267099,COSV53486315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=536;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660726,COSV53267099,COSV53486315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=131;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660726,COSV53267099,COSV53486315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1444;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1152	785	262	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1035	785	262	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	784	425	142	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	784	425	142	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	784	425	142	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1038	785	262	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1092	785	262	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1035	785	262	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1045	785	262	P/X	cCa/ca	rs876660726,COSV53267099,COSV53486315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
233908	17:7673717-7673718	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs876660726,COSV53267099,COSV53486315	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1044-1045	902-903	301	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	902-903	902-903	301	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs876660726,COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1035-1036	902-903	301	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1038-1039	902-903	301	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1035-1036	902-903	301	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660726,COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1511;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	784-785	506-507	169	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	784-785	506-507	169	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660726,COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=808;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660726,COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1398;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	638-639	506-507	169	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	784-785	506-507	169	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660726,COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660726,COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=536;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660726,COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=130;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660726,COSV53177081	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1444;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1152-1153	785-786	262	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1035-1036	785-786	262	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	784-785	425-426	142	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	784-785	425-426	142	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	784-785	425-426	142	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1038-1039	785-786	262	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1092-1093	785-786	262	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1035-1036	785-786	262	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1045-1046	785-786	262	P/PX	cca/ccCCa	rs876660726,COSV53177081	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
650927	17:7673717-7673717	GG	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs876660726,COSV53177081	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1030-1034	888-892	296-298	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	888-892	888-892	296-298	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567547030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1021-1025	888-892	296-298	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1024-1028	888-892	296-298	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1021-1025	888-892	296-298	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1497;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	770-774	492-496	164-166	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	770-774	492-496	164-166	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=794;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1384;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	624-628	492-496	164-166	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	770-774	492-496	164-166	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=485;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567547030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=141;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1430;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1138-1142	771-775	257-259	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1021-1025	771-775	257-259	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	770-774	411-415	137-139	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	770-774	411-415	137-139	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	770-774	411-415	137-139	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1024-1028	771-775	257-259	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1078-1082	771-775	257-259	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1021-1025	771-775	257-259	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1031-1035	771-775	257-259	HHE/QX	caCCACGag/caag	rs1567547030	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634763	17:7673727-7673732	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567547030	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1034	892	298	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	892	892	298	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1025	892	298	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1028	892	298	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1025	892	298	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1501;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	774	496	166	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	774	496	166	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=798;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1388;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	628	496	166	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	774	496	166	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=489;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=526;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=141;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1434;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1142	775	259	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1025	775	259	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	774	415	139	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	774	415	139	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	774	415	139	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1028	775	259	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1082	775	259	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1025	775	259	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1035	775	259	E/X	Gag/ag	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
982969	17:7673727-7673728	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1033-1034	891-892	297-298	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	891-892	891-892	297-298	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1024-1025	891-892	297-298	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1027-1028	891-892	297-298	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1024-1025	891-892	297-298	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1500;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	773-774	495-496	165-166	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	773-774	495-496	165-166	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=797;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1387;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	627-628	495-496	165-166	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	773-774	495-496	165-166	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=488;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=525;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=141;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1433;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1141-1142	774-775	258-259	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1024-1025	774-775	258-259	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	773-774	414-415	138-139	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	773-774	414-415	138-139	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	773-774	414-415	138-139	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1027-1028	774-775	258-259	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1081-1082	774-775	258-259	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1024-1025	774-775	258-259	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1034-1035	774-775	258-259	-/X	-/C	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1331829	17:7673728-7673728	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1034	892	298	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	892	892	298	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	1025	892	298	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1028	892	298	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	1025	892	298	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1501;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	774	496	166	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	774	496	166	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=798;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1388;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	628	496	166	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	774	496	166	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=489;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=526;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=141;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1434;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1142	775	259	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	1025	775	259	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	774	415	139	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	774	415	139	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	774	415	139	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1028	775	259	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1082	775	259	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	1025	775	259	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1035	775	259	E/*	Gag/Tag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
93323	17:7673728-7673728	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1032-1033	890-891	297	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	890-891	890-891	297	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV105028849,COSV52757678	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1023-1024	890-891	297	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1026-1027	890-891	297	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1023-1024	890-891	297	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105028849,COSV52757678	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1499;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	772-773	494-495	165	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	772-773	494-495	165	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105028849,COSV52757678	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=796;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105028849,COSV52757678	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1386;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	626-627	494-495	165	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	772-773	494-495	165	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105028849,COSV52757678	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=487;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105028849,COSV52757678	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=524;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105028849,COSV52757678	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=142;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105028849,COSV52757678	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1432;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1140-1141	773-774	258	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1023-1024	773-774	258	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	772-773	413-414	138	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	772-773	413-414	138	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	772-773	413-414	138	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1026-1027	773-774	258	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1080-1081	773-774	258	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1023-1024	773-774	258	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1033-1034	773-774	258	H/QERGASPX	cac/caAGAAAGGGGAGCCTCACCAc	COSV105028849,COSV52757678	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068830	17:7673729-7673729	TGGTGAGGCTCCCCTTTCT	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV105028849,COSV52757678	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1;PHENO=1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1032	890	297	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	890	890	297	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV105877278,COSV52864048,COSV53170241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1023	890	297	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1026	890	297	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1023	890	297	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105877278,COSV52864048,COSV53170241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1499;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	772	494	165	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	772	494	165	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105877278,COSV52864048,COSV53170241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=796;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105877278,COSV52864048,COSV53170241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1386;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	626	494	165	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	772	494	165	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105877278,COSV52864048,COSV53170241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=487;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105877278,COSV52864048,COSV53170241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=524;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877278,COSV52864048,COSV53170241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=143;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105877278,COSV52864048,COSV53170241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1432;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1140	773	258	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1023	773	258	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	772	413	138	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	772	413	138	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	772	413	138	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1026	773	258	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1080	773	258	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1023	773	258	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1033	773	258	H/X	cAc/cc	COSV105877278,COSV52864048,COSV53170241	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1765076	17:7673729-7673730	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV105877278,COSV52864048,COSV53170241	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1,1;PHENO=1,1,1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	987-1031	845-889	282-297	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	845-889	845-889	282-297	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567547066	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	978-1022	845-889	282-297	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	981-1025	845-889	282-297	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	978-1022	845-889	282-297	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547066	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1454;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	727-771	449-493	150-165	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	727-771	449-493	150-165	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547066	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=751;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547066	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1341;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	581-625	449-493	150-165	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	727-771	449-493	150-165	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547066	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=442;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547066	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=479;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567547066	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=144;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547066	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1387;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	1095-1139	728-772	243-258	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	978-1022	728-772	243-258	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000610623.4	Transcript	inframe_deletion	727-771	368-412	123-138	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000618944.4	Transcript	inframe_deletion	727-771	368-412	123-138	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000619186.4	Transcript	inframe_deletion	727-771	368-412	123-138	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	981-1025	728-772	243-258	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	1035-1079	728-772	243-258	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	978-1022	728-772	243-258	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	988-1032	728-772	243-258	RRTEEENLRKKGEPHH/H	cGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCac/cac	rs1567547066	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634667	17:7673730-7673775	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567547066	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1022-1023	880-881	294	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	880-881	880-881	294	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV99037302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1013-1014	880-881	294	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1016-1017	880-881	294	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1013-1014	880-881	294	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99037302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1489;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	762-763	484-485	162	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	762-763	484-485	162	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99037302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=786;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99037302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1376;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	616-617	484-485	162	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	762-763	484-485	162	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99037302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=477;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99037302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=514;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99037302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=152;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99037302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1422;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1130-1131	763-764	255	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1013-1014	763-764	255	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	762-763	403-404	135	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	762-763	403-404	135	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	762-763	403-404	135	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1016-1017	763-764	255	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1070-1071	763-764	255	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1013-1014	763-764	255	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1023-1024	763-764	255	E/GX	gag/gGag	COSV99037302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1456765	17:7673739-7673739	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV99037302	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1;PHENO=1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	1022	880	294	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	880	880	294	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	1013	880	294	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	1016	880	294	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	1013	880	294	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1489;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	762	484	162	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	762	484	162	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=786;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1376;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	616	484	162	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	762	484	162	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=477;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=514;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=153;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1422;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1130	763	255	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	1013	763	255	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	762	403	135	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	762	403	135	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	762	403	135	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	1016	763	255	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1070	763	255	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	1013	763	255	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	1023	763	255	E/*	Gag/Tag	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379471	17:7673740-7673740	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057520607,CM144128,COSV52689734,COSV52701760,COSV52773998,COSV53851434	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1012-1015	870-873	290-291	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	870-873	870-873	290-291	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1003-1006	870-873	290-291	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1006-1009	870-873	290-291	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1003-1006	870-873	290-291	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1479;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	752-755	474-477	158-159	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	752-755	474-477	158-159	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=776;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1366;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	606-609	474-477	158-159	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	752-755	474-477	158-159	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=467;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=160;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1412;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1120-1123	753-756	251-252	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1003-1006	753-756	251-252	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	752-755	393-396	131-132	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	752-755	393-396	131-132	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	752-755	393-396	131-132	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1006-1009	753-756	251-252	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1060-1063	753-756	251-252	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1003-1006	753-756	251-252	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1013-1016	753-756	251-252	RK/X	cgCAAG/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853645	17:7673746-7673750	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1012-1013	870-871	290-291	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	870-871	870-871	290-291	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1003-1004	870-871	290-291	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1006-1007	870-871	290-291	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1003-1004	870-871	290-291	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1479;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	752-753	474-475	158-159	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	752-753	474-475	158-159	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=776;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1366;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	606-607	474-475	158-159	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	752-753	474-475	158-159	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=467;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=162;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1412;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1120-1121	753-754	251-252	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1003-1004	753-754	251-252	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	752-753	393-394	131-132	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	752-753	393-394	131-132	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	752-753	393-394	131-132	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1006-1007	753-754	251-252	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1060-1061	753-754	251-252	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1003-1004	753-754	251-252	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1013-1014	753-754	251-252	-/X	-/C	rs1555525140	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458573	17:7673749-7673749	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525140	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1010	868	290	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	868	868	290	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1001	868	290	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1004	868	290	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1001	868	290	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1477;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	750	472	158	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	750	472	158	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1364;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	604	472	158	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	750	472	158	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=465;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=165;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1410;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1118	751	251	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1001	751	251	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	750	391	131	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	750	391	131	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	750	391	131	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1004	751	251	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1058	751	251	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1001	751	251	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1011	751	251	R/X	Cgc/gc	COSV52761356,COSV53509681	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1452408	17:7673751-7673752	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52761356,COSV53509681	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1;PHENO=1,1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1009-1010	867-868	289-290	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	867-868	867-868	289-290	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597360991	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	1000-1001	867-868	289-290	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	1003-1004	867-868	289-290	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	1000-1001	867-868	289-290	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360991	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1476;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	749-750	471-472	157-158	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	749-750	471-472	157-158	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360991	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=773;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360991	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1363;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	603-604	471-472	157-158	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	749-750	471-472	157-158	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360991	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=464;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360991	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597360991	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=165;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597360991	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1409;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1117-1118	750-751	250-251	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	1000-1001	750-751	250-251	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	749-750	390-391	130-131	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	749-750	390-391	130-131	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	749-750	390-391	130-131	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	1003-1004	750-751	250-251	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1057-1058	750-751	250-251	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	1000-1001	750-751	250-251	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1010-1011	750-751	250-251	-/AQRKRIX	-/GCACAGAGGAAGAGAATCTC	rs1597360991	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
650094	17:7673752-7673752	GAGATTCTCTTCCTCTGTGC	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597360991	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1005	863	288	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	863	863	288	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52712952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	996	863	288	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	999	863	288	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	996	863	288	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1472;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	745	467	156	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	745	467	156	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=769;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1359;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	599	467	156	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	745	467	156	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=460;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=497;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52712952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=170;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1405;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1113	746	249	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	996	746	249	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	745	386	129	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	745	386	129	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	745	386	129	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	999	746	249	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1053	746	249	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	996	746	249	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1006	746	249	N/X	aAt/at	COSV52712952	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1391991	17:7673756-7673757	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52712952	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1;PHENO=1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1005-1006	863-864	288	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	863-864	863-864	288	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525156,COSV99387464	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	996-997	863-864	288	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	999-1000	863-864	288	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	996-997	863-864	288	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525156,COSV99387464	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1472;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	745-746	467-468	156	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	745-746	467-468	156	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525156,COSV99387464	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=769;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525156,COSV99387464	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1359;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	599-600	467-468	156	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	745-746	467-468	156	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525156,COSV99387464	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=460;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525156,COSV99387464	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=497;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525156,COSV99387464	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=169;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525156,COSV99387464	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1405;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1113-1114	746-747	249	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	996-997	746-747	249	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	745-746	386-387	129	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	745-746	386-387	129	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	745-746	386-387	129	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	999-1000	746-747	249	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1053-1054	746-747	249	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	996-997	746-747	249	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1006-1007	746-747	249	N/KAQRKRX	aat/aaGGCACAGAGGAAGAGAAt	rs1555525156,COSV99387464	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
485041	17:7673756-7673756	TTCTCTTCCTCTGTGCC	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525156,COSV99387464	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,1;PHENO=1,1
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	985-1004	843-862	281-288	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	843-862	843-862	281-288	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	976-995	843-862	281-288	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	979-998	843-862	281-288	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	976-995	843-862	281-288	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1452;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	725-744	447-466	149-156	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	725-744	447-466	149-156	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=749;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1339;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	579-598	447-466	149-156	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	725-744	447-466	149-156	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=440;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=477;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=171;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1385;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1093-1112	726-745	242-249	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	976-995	726-745	242-249	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	725-744	366-385	122-129	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	725-744	366-385	122-129	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	725-744	366-385	122-129	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	979-998	726-745	242-249	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1033-1052	726-745	242-249	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	976-995	726-745	242-249	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	986-1005	726-745	242-249	DRRTEEEN/EX	gaCCGGCGCACAGAGGAAGAGAat/gaat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1763362	17:7673757-7673777	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	1004-1005	862-863	288	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	862-863	862-863	288	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525158,COSV53024645	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	995-996	862-863	288	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	998-999	862-863	288	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	995-996	862-863	288	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525158,COSV53024645	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1471;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	744-745	466-467	156	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	744-745	466-467	156	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525158,COSV53024645	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=768;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525158,COSV53024645	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1358;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	598-599	466-467	156	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	744-745	466-467	156	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525158,COSV53024645	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=459;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525158,COSV53024645	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525158,COSV53024645	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=170;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525158,COSV53024645	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1404;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1112-1113	745-746	249	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	995-996	745-746	249	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	744-745	385-386	129	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	744-745	385-386	129	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	744-745	385-386	129	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	998-999	745-746	249	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1052-1053	745-746	249	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	995-996	745-746	249	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	1005-1006	745-746	249	N/RX	aat/aGAat	rs1555525158,COSV53024645	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
481127	17:7673757-7673757	TC	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525158,COSV53024645	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,1;PHENO=1,1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	990-999	848-857	283-286	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	848-857	848-857	283-286	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	981-990	848-857	283-286	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	984-993	848-857	283-286	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	981-990	848-857	283-286	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1457;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	730-739	452-461	151-154	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	730-739	452-461	151-154	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=754;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1344;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	584-593	452-461	151-154	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	730-739	452-461	151-154	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=445;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=482;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=176;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1390;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1098-1107	731-740	244-247	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	981-990	731-740	244-247	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	730-739	371-380	124-127	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	730-739	371-380	124-127	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	730-739	371-380	124-127	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	984-993	731-740	244-247	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1038-1047	731-740	244-247	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	981-990	731-740	244-247	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	991-1000	731-740	244-247	RTEE/X	cGCACAGAGGAa/ca	rs1555525170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458569	17:7673762-7673772	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525170	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	999	857	286	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	857	857	286	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	990	857	286	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	993	857	286	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	990	857	286	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1466;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	739	461	154	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	739	461	154	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=763;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1353;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	593	461	154	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	739	461	154	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=454;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=491;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=176;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1399;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1107	740	247	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	990	740	247	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	739	380	127	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	739	380	127	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	739	380	127	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	993	740	247	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1047	740	247	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	990	740	247	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1000	740	247	E/V	gAa/gTa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376592	17:7673763-7673763	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	999	857	286	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	857	857	286	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	990	857	286	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	993	857	286	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	990	857	286	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1466;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	739	461	154	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	739	461	154	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=763;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1353;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	593	461	154	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	739	461	154	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=454;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=491;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=176;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1399;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1107	740	247	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	990	740	247	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	739	380	127	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	739	380	127	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	739	380	127	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	993	740	247	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1047	740	247	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	990	740	247	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1000	740	247	E/A	gAa/gCa	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376593	17:7673763-7673763	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057519985,CM920679,COSV52661405,COSV52748431,COSV53044704	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	995-998	853-856	285-286	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	853-856	853-856	285-286	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	986-989	853-856	285-286	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	989-992	853-856	285-286	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	986-989	853-856	285-286	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1462;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	735-738	457-460	153-154	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	735-738	457-460	153-154	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1349;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	589-592	457-460	153-154	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	735-738	457-460	153-154	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=450;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=487;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=177;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1395;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1103-1106	736-739	246-247	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	986-989	736-739	246-247	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	735-738	376-379	126-127	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	735-738	376-379	126-127	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	735-738	376-379	126-127	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	989-992	736-739	246-247	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1043-1046	736-739	246-247	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	986-989	736-739	246-247	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	996-999	736-739	246-247	EE/X	GAGGaa/aa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
849951	17:7673763-7673767	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	998	856	286	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	856	856	286	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	989	856	286	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	992	856	286	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	989	856	286	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1465;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	738	460	154	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	738	460	154	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=762;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1352;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	592	460	154	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	738	460	154	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=453;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=490;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=177;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1398;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1106	739	247	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	989	739	247	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	738	379	127	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	738	379	127	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	738	379	127	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	992	739	247	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1046	739	247	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	989	739	247	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	999	739	247	E/*	Gaa/Taa	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634755	17:7673764-7673764	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs786201059,CM076567,CM1212545,COSV52664318,COSV52687201,COSV52688214	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	993-997	851-855	284-285	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	851-855	851-855	284-285	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	984-988	851-855	284-285	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	987-991	851-855	284-285	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	984-988	851-855	284-285	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1460;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	733-737	455-459	152-153	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	733-737	455-459	152-153	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=757;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1347;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	587-591	455-459	152-153	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	733-737	455-459	152-153	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=448;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=485;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=178;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1393;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1101-1105	734-738	245-246	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	984-988	734-738	245-246	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	733-737	374-378	125-126	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	733-737	374-378	125-126	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	733-737	374-378	125-126	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	987-991	734-738	245-246	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1041-1045	734-738	245-246	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	984-988	734-738	245-246	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	994-998	734-738	245-246	TE/X	aCAGAG/a	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984965	17:7673764-7673769	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	969-995	827-853	276-285	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	827-853	827-853	276-285	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	960-986	827-853	276-285	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	963-989	827-853	276-285	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	960-986	827-853	276-285	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1436;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	709-735	431-457	144-153	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	709-735	431-457	144-153	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=733;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1323;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	563-589	431-457	144-153	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	709-735	431-457	144-153	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=424;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=461;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=180;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1369;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	1077-1103	710-736	237-246	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	960-986	710-736	237-246	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000610623.4	Transcript	inframe_deletion	709-735	350-376	117-126	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000618944.4	Transcript	inframe_deletion	709-735	350-376	117-126	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000619186.4	Transcript	inframe_deletion	709-735	350-376	117-126	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	963-989	710-736	237-246	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	1017-1043	710-736	237-246	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	960-986	710-736	237-246	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	970-996	710-736	237-246	ACPGRDRRTE/E	gCCTGTCCTGGGAGAGACCGGCGCACAGag/gag	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1210119	17:7673766-7673793	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	995	853	285	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	853	853	285	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	986	853	285	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	989	853	285	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	986	853	285	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1462;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	735	457	153	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	735	457	153	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1349;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	589	457	153	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	735	457	153	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=450;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=487;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=180;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1395;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1103	736	246	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	986	736	246	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	735	376	126	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	735	376	126	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	735	376	126	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	989	736	246	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1043	736	246	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	986	736	246	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	996	736	246	E/K	Gag/Aag	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
420133	17:7673767-7673767	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs112431538,CM123560,CM995136,COSV52661732,COSV52670664,COSV53234441,COSV53650254	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=drug_response,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	992	850	284	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	850	850	284	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	983	850	284	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	986	850	284	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	983	850	284	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1459;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	732	454	152	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	732	454	152	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=756;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1346;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	586	454	152	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	732	454	152	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=447;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=484;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=183;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1392;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1100	733	245	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	983	733	245	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	732	373	125	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	732	373	125	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	732	373	125	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	986	733	245	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1040	733	245	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	983	733	245	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	993	733	245	T/P	Aca/Cca	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1763670	17:7673770-7673770	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1204379654,CM156903,COSV52809281,COSV52896079,COSV53120916,COSV53272353	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	990-991	848-849	283	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	848-849	848-849	283	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	981-982	848-849	283	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	984-985	848-849	283	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	981-982	848-849	283	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1457;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	730-731	452-453	151	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	730-731	452-453	151	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=754;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1344;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	584-585	452-453	151	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	730-731	452-453	151	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=445;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=482;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=184;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1390;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1098-1099	731-732	244	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	981-982	731-732	244	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	730-731	371-372	124	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	730-731	371-372	124	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	730-731	371-372	124	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	984-985	731-732	244	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1038-1039	731-732	244	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	981-982	731-732	244	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	991-992	731-732	244	R/X	cGC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984964	17:7673770-7673772	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000269305.9	Transcript	protein_altering_variant	980-990	838-848	280-283	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000359597.8	Transcript	protein_altering_variant	838-848	838-848	280-283	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587781564	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000420246.6	Transcript	protein_altering_variant	971-981	838-848	280-283	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000445888.6	Transcript	protein_altering_variant	974-984	838-848	280-283	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000455263.6	Transcript	protein_altering_variant	971-981	838-848	280-283	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781564	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1447;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000504290.5	Transcript	protein_altering_variant	720-730	442-452	148-151	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000504937.5	Transcript	protein_altering_variant	720-730	442-452	148-151	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781564	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=744;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781564	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1334;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000509690.5	Transcript	protein_altering_variant	574-584	442-452	148-151	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000510385.5	Transcript	protein_altering_variant	720-730	442-452	148-151	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781564	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=435;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781564	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=472;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781564	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=185;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781564	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1380;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000610292.4	Transcript	protein_altering_variant	1088-1098	721-731	241-244	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000610538.4	Transcript	protein_altering_variant	971-981	721-731	241-244	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000610623.4	Transcript	protein_altering_variant	720-730	361-371	121-124	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000618944.4	Transcript	protein_altering_variant	720-730	361-371	121-124	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000619186.4	Transcript	protein_altering_variant	720-730	361-371	121-124	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000619485.4	Transcript	protein_altering_variant	974-984	721-731	241-244	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000620739.4	Transcript	protein_altering_variant	1028-1038	721-731	241-244	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000622645.4	Transcript	protein_altering_variant	971-981	721-731	241-244	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	ENSG00000141510	ENST00000635293.1	Transcript	protein_altering_variant,NMD_transcript_variant	981-991	721-731	241-244	RDRR/H	AGAGACCGGCGc/CAc	rs587781564	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
141193	17:7673772-7673782	TG	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs587781564	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic;PHENO=1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	989-990	847-848	283	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	847-848	847-848	283	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV53297573,COSV99037230	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	980-981	847-848	283	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	983-984	847-848	283	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	980-981	847-848	283	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53297573,COSV99037230	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1456;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	729-730	451-452	151	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	729-730	451-452	151	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53297573,COSV99037230	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=753;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53297573,COSV99037230	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1343;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	583-584	451-452	151	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	729-730	451-452	151	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53297573,COSV99037230	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=444;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53297573,COSV99037230	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=481;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53297573,COSV99037230	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=185;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53297573,COSV99037230	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1389;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1097-1098	730-731	244	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	980-981	730-731	244	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	729-730	370-371	124	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	729-730	370-371	124	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	729-730	370-371	124	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	983-984	730-731	244	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1037-1038	730-731	244	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	980-981	730-731	244	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	990-991	730-731	244	R/PX	cgc/cCgc	COSV53297573,COSV99037230	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1457232	17:7673772-7673772	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV53297573,COSV99037230	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1;PHENO=1,1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	986-989	844-847	282-283	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	844-847	844-847	282-283	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525209	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	977-980	844-847	282-283	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	980-983	844-847	282-283	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	977-980	844-847	282-283	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525209	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1453;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	726-729	448-451	150-151	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	726-729	448-451	150-151	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525209	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=750;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525209	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1340;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	580-583	448-451	150-151	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	726-729	448-451	150-151	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525209	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=441;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525209	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=478;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525209	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=186;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525209	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1386;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1094-1097	727-730	243-244	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	977-980	727-730	243-244	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	726-729	367-370	123-124	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	726-729	367-370	123-124	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	726-729	367-370	123-124	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	980-983	727-730	243-244	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1034-1037	727-730	243-244	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	977-980	727-730	243-244	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	987-990	727-730	243-244	RR/RX	CGGCgc/AGgc	rs1555525209	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528267	17:7673773-7673776	CT	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525209	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;PHENO=1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	987	845	282	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	845	845	282	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	978	845	282	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	981	845	282	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	978	845	282	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1454;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	727	449	150	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	727	449	150	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=751;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1341;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	581	449	150	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	727	449	150	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=442;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=479;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=188;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1387;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1095	728	243	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	978	728	243	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	727	368	123	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	727	368	123	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	727	368	123	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	981	728	243	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1035	728	243	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	978	728	243	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	988	728	243	R/P	cGg/cCg	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376659	17:7673775-7673775	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs730882008,CM004344,CM1612889,COSV52689673,COSV52773873,COSV52969460,COSV53068318	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic/likely_pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	986	844	282	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	844	844	282	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	977	844	282	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	980	844	282	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	977	844	282	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1453;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	726	448	150	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	726	448	150	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=750;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1340;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	580	448	150	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	726	448	150	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=441;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=478;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=189;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1386;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1094	727	243	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	977	727	243	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	726	367	123	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	726	367	123	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	726	367	123	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	980	727	243	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1034	727	243	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	977	727	243	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	987	727	243	R/X	Cgg/gg	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428891	17:7673775-7673776	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1131691027,CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	984-985	842-843	281	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	842-843	842-843	281	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	975-976	842-843	281	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	978-979	842-843	281	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	975-976	842-843	281	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1451;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	724-725	446-447	149	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	724-725	446-447	149	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1338;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	578-579	446-447	149	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	724-725	446-447	149	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=439;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=476;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=190;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1384;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1092-1093	725-726	242	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	975-976	725-726	242	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	724-725	365-366	122	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	724-725	365-366	122	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	724-725	365-366	122	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	978-979	725-726	242	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1032-1033	725-726	242	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	975-976	725-726	242	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	985-986	725-726	242	D/EX	gac/gaGc	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
485037	17:7673777-7673777	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525226,COSV104584625,COSV52873430,COSV52898385,COSV53426350	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	983-984	841-842	281	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	841-842	841-842	281	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567547661	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	974-975	841-842	281	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	977-978	841-842	281	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	974-975	841-842	281	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547661	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1450;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	723-724	445-446	149	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	723-724	445-446	149	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547661	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547661	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1337;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	577-578	445-446	149	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	723-724	445-446	149	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547661	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=438;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547661	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=475;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567547661	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=191;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547661	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1383;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1091-1092	724-725	242	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	974-975	724-725	242	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	723-724	364-365	122	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	723-724	364-365	122	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	723-724	364-365	122	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	977-978	724-725	242	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1031-1032	724-725	242	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	974-975	724-725	242	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	984-985	724-725	242	D/X	GAc/c	rs1567547661	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
570804	17:7673777-7673779	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567547661	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;PHENO=1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	984	842	281	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	842	842	281	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	975	842	281	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	978	842	281	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	975	842	281	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1451;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	724	446	149	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	724	446	149	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1338;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	578	446	149	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	724	446	149	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=439;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=476;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=191;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1384;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1092	725	242	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	975	725	242	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	724	365	122	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	724	365	122	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	724	365	122	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	978	725	242	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1032	725	242	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	975	725	242	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	985	725	242	D/A	gAc/gCc	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376589	17:7673778-7673778	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs587781525,CM004343,CM056068,CM114008,COSV52694391,COSV52729448,COSV52815868	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	983	841	281	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	841	841	281	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	974	841	281	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	977	841	281	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	974	841	281	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1450;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	723	445	149	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	723	445	149	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1337;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	577	445	149	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	723	445	149	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=438;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=475;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=192;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1383;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1091	724	242	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	974	724	242	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	723	364	122	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	723	364	122	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	723	364	122	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	977	724	242	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1031	724	242	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	974	724	242	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	984	724	242	D/Y	Gac/Tac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376585	17:7673779-7673779	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	983	841	281	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	841	841	281	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	974	841	281	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	977	841	281	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	974	841	281	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1450;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	723	445	149	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	723	445	149	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1337;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	577	445	149	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	723	445	149	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=438;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=475;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=192;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1383;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1091	724	242	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	974	724	242	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	723	364	122	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	723	364	122	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	723	364	122	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	977	724	242	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1031	724	242	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	974	724	242	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	984	724	242	D/N	Gac/Aac	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
376586	17:7673779-7673779	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs764146326,CD137626,CM076566,CM153816,COSV52671054,COSV52674651,COSV52678614	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1;PHENO=1,1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	981	839	280	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	839	839	280	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	972	839	280	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	975	839	280	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	972	839	280	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1448;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	721	443	148	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	721	443	148	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=745;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1335;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	575	443	148	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	721	443	148	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=436;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=473;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=194;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1381;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1089	722	241	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	972	722	241	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	721	362	121	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	721	362	121	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	721	362	121	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	975	722	241	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1029	722	241	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	972	722	241	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	982	722	241	R/X	aGa/aa	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
628117	17:7673780-7673781	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567547721,CM153865,CM993218,COSV52666248,COSV52677783,COSV52687987	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	982	840	280	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	840	840	280	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	973	840	280	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	976	840	280	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	973	840	280	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1449;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	722	444	148	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	722	444	148	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=746;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1336;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	576	444	148	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	722	444	148	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=437;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=474;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=193;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1382;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1090	723	241	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	973	723	241	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	722	363	121	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	722	363	121	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	722	363	121	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	976	723	241	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1030	723	241	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	973	723	241	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	983	723	241	R/S	agA/agT	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
988616	17:7673780-7673780	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	CM136794,COSV52678283,COSV52782181,COSV52801834,COSV53205654	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	973-977	831-835	277-279	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	831-835	831-835	277-279	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	964-968	831-835	277-279	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	967-971	831-835	277-279	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	964-968	831-835	277-279	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1440;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	713-717	435-439	145-147	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	713-717	435-439	145-147	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=737;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1327;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	567-571	435-439	145-147	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	713-717	435-439	145-147	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=428;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=465;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=198;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1373;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1081-1085	714-718	238-240	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	964-968	714-718	238-240	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	713-717	354-358	118-120	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	713-717	354-358	118-120	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	713-717	354-358	118-120	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	967-971	714-718	238-240	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1021-1025	714-718	238-240	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	964-968	714-718	238-240	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	974-978	714-718	238-240	CPG/WX	tgTCCTGgg/tggg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453992	17:7673784-7673789	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	978	836	279	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	836	836	279	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	969	836	279	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	972	836	279	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	969	836	279	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1445;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	718	440	147	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	718	440	147	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=742;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1332;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	572	440	147	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	718	440	147	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=433;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=470;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=197;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1378;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1086	719	240	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	969	719	240	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	718	359	120	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	718	359	120	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	718	359	120	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	972	719	240	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1026	719	240	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	969	719	240	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	979	719	240	G/E	gGg/gAg	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419454	17:7673784-7673784	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1064793881,COSV52677880,COSV52851240	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	958-973	816-831	272-277	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	816-831	816-831	272-277	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	949-964	816-831	272-277	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	952-967	816-831	272-277	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	949-964	816-831	272-277	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1425;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	698-713	420-435	140-145	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	698-713	420-435	140-145	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1312;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	552-567	420-435	140-145	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	698-713	420-435	140-145	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=413;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=450;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=202;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1358;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1066-1081	699-714	233-238	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	949-964	699-714	233-238	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	698-713	339-354	113-118	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	698-713	339-354	113-118	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	698-713	339-354	113-118	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	952-967	699-714	233-238	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1006-1021	699-714	233-238	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	949-964	699-714	233-238	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	959-974	699-714	233-238	VRVCAC/X	gtGCGTGTTTGTGCCTGT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1456701	17:7673788-7673804	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	974	832	278	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	832	832	278	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	965	832	278	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	968	832	278	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	965	832	278	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1441;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	714	436	146	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	714	436	146	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=738;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1328;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	568	436	146	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	714	436	146	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=429;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=466;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=201;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1374;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1082	715	239	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	965	715	239	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	714	355	119	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	714	355	119	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	714	355	119	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	968	715	239	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1022	715	239	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	965	715	239	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	975	715	239	P/T	Cct/Act	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
376643	17:7673788-7673788	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs17849781,CM011015,CM052927,CM120850,CX0910928,COSV52668132,COSV52679740,COSV52684662,COSV52950563	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=drug_response,likely_pathogenic;SOMATIC=0,0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	973	831	277	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	831	831	277	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	964	831	277	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	967	831	277	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	964	831	277	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1440;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	713	435	145	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	713	435	145	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=737;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1327;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	567	435	145	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	713	435	145	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=428;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=465;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=202;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1373;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1081	714	238	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	964	714	238	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	713	354	118	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	713	354	118	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	713	354	118	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	967	714	238	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1021	714	238	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	964	714	238	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	974	714	238	C/*	tgT/tgA	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
492746	17:7673789-7673789	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	956-968	814-826	272-276	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	814-826	814-826	272-276	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	947-959	814-826	272-276	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	950-962	814-826	272-276	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	947-959	814-826	272-276	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1423;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	696-708	418-430	140-144	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	696-708	418-430	140-144	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1310;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	550-562	418-430	140-144	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	696-708	418-430	140-144	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=411;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=448;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=207;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1356;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1064-1076	697-709	233-237	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	947-959	697-709	233-237	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	696-708	337-349	113-117	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	696-708	337-349	113-117	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	696-708	337-349	113-117	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	950-962	697-709	233-237	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1004-1016	697-709	233-237	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	947-959	697-709	233-237	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	957-969	697-709	233-237	VRVCA/X	GTGCGTGTTTGTGcc/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076516	17:7673793-7673806	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	967	825	275	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	825	825	275	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	958	825	275	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	961	825	275	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	958	825	275	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1434;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	707	429	143	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	707	429	143	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1321;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	561	429	143	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	707	429	143	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=422;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=459;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=208;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1367;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1075	708	236	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	958	708	236	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	707	348	116	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	707	348	116	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	707	348	116	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	961	708	236	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1015	708	236	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	958	708	236	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	968	708	236	C/X	tgT/tg	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1453085	17:7673794-7673795	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	967	825	275	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	825	825	275	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	958	825	275	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	961	825	275	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	958	825	275	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1434;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	707	429	143	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	707	429	143	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1321;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	561	429	143	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	707	429	143	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=422;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=459;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=208;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1367;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1075	708	236	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	958	708	236	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	707	348	116	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	707	348	116	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	707	348	116	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	961	708	236	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1015	708	236	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	958	708	236	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	968	708	236	C/*	tgT/tgA	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1012210	17:7673795-7673795	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	967	825	275	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	825	825	275	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	958	825	275	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	961	825	275	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	958	825	275	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1434;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	707	429	143	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	707	429	143	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1321;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	561	429	143	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	707	429	143	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=422;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=459;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=208;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1367;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1075	708	236	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	958	708	236	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	707	348	116	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	707	348	116	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	707	348	116	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	961	708	236	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1015	708	236	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	958	708	236	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	968	708	236	C/W	tgT/tgG	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485044	17:7673795-7673795	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525279,CM152980,COSV52759232,COSV52912941,COSV53086963	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	966	824	275	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	824	824	275	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	957	824	275	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	960	824	275	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	957	824	275	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1433;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	706	428	143	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	706	428	143	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=730;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1320;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	560	428	143	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	706	428	143	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=421;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=458;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=209;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1366;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1074	707	236	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	957	707	236	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	706	347	116	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	706	347	116	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	706	347	116	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	960	707	236	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1014	707	236	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	957	707	236	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	967	707	236	C/F	tGt/tTt	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376582	17:7673796-7673796	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs863224451,CM076568,CM951234,COSV52661919,COSV52663595,COSV52675710,COSV52772708	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	965	823	275	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	823	823	275	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	956	823	275	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	959	823	275	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	956	823	275	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1432;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	705	427	143	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	705	427	143	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=729;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1319;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	559	427	143	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	705	427	143	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=420;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=457;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=210;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1365;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1073	706	236	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	956	706	236	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	705	346	116	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	705	346	116	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	705	346	116	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	959	706	236	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1013	706	236	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	956	706	236	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	966	706	236	C/R	Tgt/Cgt	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376584	17:7673797-7673797	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057519983,COSV104585223,COSV52700773,COSV52771673	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	962-963	820-821	274	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	820-821	820-821	274	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567547933	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	953-954	820-821	274	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	956-957	820-821	274	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	953-954	820-821	274	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547933	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1429;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	702-703	424-425	142	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	702-703	424-425	142	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547933	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=726;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547933	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1316;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	556-557	424-425	142	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	702-703	424-425	142	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547933	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=417;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547933	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=454;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567547933	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=212;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567547933	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1362;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1070-1071	703-704	235	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	953-954	703-704	235	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	702-703	343-344	115	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	702-703	343-344	115	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	702-703	343-344	115	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	956-957	703-704	235	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1010-1011	703-704	235	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	953-954	703-704	235	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	963-964	703-704	235	V/X	GTt/t	rs1567547933	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
575419	17:7673798-7673800	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567547933	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	950-959	808-817	270-273	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	808-817	808-817	270-273	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587781987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	941-950	808-817	270-273	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	944-953	808-817	270-273	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	941-950	808-817	270-273	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1417;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	690-699	412-421	138-141	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	690-699	412-421	138-141	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=714;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1304;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	544-553	412-421	138-141	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	690-699	412-421	138-141	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=405;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=442;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=216;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781987	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1350;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1058-1067	691-700	231-234	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	941-950	691-700	231-234	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	690-699	331-340	111-114	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	690-699	331-340	111-114	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	690-699	331-340	111-114	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	944-953	691-700	231-234	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	998-1007	691-700	231-234	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	941-950	691-700	231-234	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
141756	17:7673802-7673812	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	951-960	691-700	231-234	FEVR/X	TTTGAGGTGCgt/gt	rs587781987	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	960	818	273	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	818	818	273	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	951	818	273	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	954	818	273	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	951	818	273	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1427;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	700	422	141	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	700	422	141	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=724;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1314;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	554	422	141	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	700	422	141	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=415;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=452;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=215;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1360;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1068	701	234	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	951	701	234	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	700	341	114	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	700	341	114	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	700	341	114	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	954	701	234	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1008	701	234	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	951	701	234	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376655	17:7673802-7673802	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	961	701	234	R/L	cGt/cTt	rs28934576,CM004342,CM010472,CM920677,COSV52660980,COSV52664805,COSV52676050,COSV52728930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	959	817	273	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	817	817	273	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	950	817	273	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	953	817	273	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	950	817	273	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1426;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	699	421	141	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	699	421	141	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=723;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1313;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	553	421	141	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	699	421	141	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=414;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=451;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=216;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1359;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1067	700	234	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	950	700	234	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	699	340	114	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	699	340	114	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	699	340	114	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	953	700	234	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1007	700	234	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	950	700	234	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376656	17:7673803-7673803	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	960	700	234	R/S	Cgt/Agt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	959	817	273	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	817	817	273	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	950	817	273	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	953	817	273	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	950	817	273	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1426;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	699	421	141	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	699	421	141	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=723;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1313;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	553	421	141	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	699	421	141	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=414;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=451;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=216;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1359;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1067	700	234	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	950	700	234	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	699	340	114	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	699	340	114	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	699	340	114	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	953	700	234	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1007	700	234	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	950	700	234	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634682	17:7673803-7673803	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	960	700	234	R/G	Cgt/Ggt	rs121913343,CM010471,CM010473,CM951233,COSV52662066,COSV52670856,COSV52707054,COSV53164203	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	957-958	815-816	272	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	815-816	815-816	272	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597362004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	948-949	815-816	272	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	951-952	815-816	272	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	948-949	815-816	272	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1424;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	697-698	419-420	140	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	697-698	419-420	140	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=721;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1311;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	551-552	419-420	140	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	697-698	419-420	140	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=412;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=449;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597362004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=217;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1357;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1065-1066	698-699	233	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	948-949	698-699	233	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	697-698	338-339	113	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	697-698	338-339	113	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	697-698	338-339	113	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	951-952	698-699	233	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1005-1006	698-699	233	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	948-949	698-699	233	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
656861	17:7673804-7673804	ACCT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	958-959	698-699	233	V/VGX	gtg/gtAGGTg	rs1597362004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	956	814	272	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	814	814	272	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	947	814	272	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	950	814	272	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	947	814	272	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1423;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	696	418	140	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	696	418	140	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1310;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	550	418	140	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	696	418	140	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=411;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=448;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=219;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1356;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1064	697	233	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	947	697	233	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	696	337	113	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	696	337	113	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	696	337	113	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	950	697	233	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1004	697	233	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	947	697	233	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
574679	17:7673806-7673806	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	957	697	233	V/L	Gtg/Ctg	rs121912657,CM130241,CM920676,COSV52661812,COSV52677483,COSV52701127	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	953	811	271	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	811	811	271	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52666332,COSV52700326,COSV52746468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	944	811	271	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	947	811	271	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	944	811	271	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52666332,COSV52700326,COSV52746468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1420;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	693	415	139	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	693	415	139	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52666332,COSV52700326,COSV52746468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52666332,COSV52700326,COSV52746468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1307;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	547	415	139	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	693	415	139	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52666332,COSV52700326,COSV52746468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=408;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52666332,COSV52700326,COSV52746468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=445;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52666332,COSV52700326,COSV52746468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=222;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52666332,COSV52700326,COSV52746468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1353;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1061	694	232	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	944	694	232	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	693	334	112	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	693	334	112	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	693	334	112	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	947	694	232	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	1001	694	232	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	944	694	232	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1174012	17:7673809-7673809	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	954	694	232	E/*	Gag/Tag	COSV52666332,COSV52700326,COSV52746468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	952	810	270	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	810	810	270	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567548114,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	943	810	270	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	946	810	270	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	943	810	270	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548114,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1419;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	692	414	138	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	692	414	138	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548114,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=716;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548114,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1306;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	546	414	138	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	692	414	138	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548114,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=407;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548114,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=444;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567548114,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=223;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548114,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1352;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1060	693	231	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	943	693	231	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	692	333	111	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	692	333	111	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	692	333	111	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	946	693	231	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1000	693	231	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	943	693	231	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634749	17:7673809-7673810	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	953	693	231	F/X	ttT/tt	rs1567548114,COSV52809003,COSV53009334	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	952-953	810-811	270-271	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	810-811	810-811	270-271	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	943-944	810-811	270-271	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	946-947	810-811	270-271	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	943-944	810-811	270-271	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1419;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	692-693	414-415	138-139	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	692-693	414-415	138-139	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=716;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1306;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	546-547	414-415	138-139	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	692-693	414-415	138-139	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=407;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=444;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=222;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1352;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1060-1061	693-694	231-232	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	943-944	693-694	231-232	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	692-693	333-334	111-112	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	692-693	333-334	111-112	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	692-693	333-334	111-112	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	946-947	693-694	231-232	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	1000-1001	693-694	231-232	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	943-944	693-694	231-232	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
856060	17:7673809-7673809	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	953-954	693-694	231-232	-/X	-/T	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	952	810	270	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	810	810	270	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	943	810	270	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	946	810	270	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	943	810	270	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1419;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	692	414	138	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	692	414	138	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=716;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1306;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	546	414	138	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	692	414	138	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=407;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=444;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=223;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1352;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1060	693	231	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	943	693	231	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	692	333	111	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	692	333	111	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	692	333	111	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	946	693	231	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1000	693	231	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	943	693	231	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376595	17:7673810-7673810	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	953	693	231	F/L	ttT/ttG	rs1057519987,COSV52809003,COSV53009334	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	938-950	796-808	266-270	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	796-808	796-808	266-270	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs886039855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	929-941	796-808	266-270	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	932-944	796-808	266-270	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	929-941	796-808	266-270	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs886039855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1405;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	678-690	400-412	134-138	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	678-690	400-412	134-138	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886039855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=702;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886039855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1292;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	532-544	400-412	134-138	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	678-690	400-412	134-138	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886039855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=393;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs886039855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=430;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs886039855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=225;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886039855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1338;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1046-1058	679-691	227-231	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	929-941	679-691	227-231	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	678-690	319-331	107-111	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	678-690	319-331	107-111	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	678-690	319-331	107-111	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	932-944	679-691	227-231	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	986-998	679-691	227-231	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	929-941	679-691	227-231	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
267321	17:7673811-7673824	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	939-951	679-691	227-231	GRNSF/X	GGACGGAACAGCTtt/tt	rs886039855	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	951	809	270	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	809	809	270	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	942	809	270	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	945	809	270	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	942	809	270	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1418;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	691	413	138	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	691	413	138	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=715;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1305;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	545	413	138	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	691	413	138	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=406;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=443;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=224;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1351;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1059	692	231	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	942	692	231	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	691	332	111	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	691	332	111	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	691	332	111	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	945	692	231	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	999	692	231	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	942	692	231	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376594	17:7673811-7673811	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	952	692	231	F/S	tTt/tCt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	951	809	270	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	809	809	270	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	942	809	270	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	945	809	270	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	942	809	270	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1418;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	691	413	138	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	691	413	138	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=715;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1305;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	545	413	138	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	691	413	138	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=406;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=443;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=224;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1351;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1059	692	231	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	942	692	231	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	691	332	111	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	691	332	111	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	691	332	111	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	945	692	231	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	999	692	231	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	942	692	231	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376597	17:7673811-7673811	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	952	692	231	F/C	tTt/tGt	rs1057519986,COSV52661272,COSV52676663,COSV52688116	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	949	807	269	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	807	807	269	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV104587891,COSV53165079,COSV53562993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	940	807	269	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	943	807	269	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	940	807	269	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104587891,COSV53165079,COSV53562993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1416;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	689	411	137	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	689	411	137	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104587891,COSV53165079,COSV53562993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=713;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104587891,COSV53165079,COSV53562993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1303;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	543	411	137	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	689	411	137	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104587891,COSV53165079,COSV53562993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=404;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104587891,COSV53165079,COSV53562993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=441;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104587891,COSV53165079,COSV53562993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=226;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104587891,COSV53165079,COSV53562993	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1349;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1057	690	230	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	940	690	230	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	689	330	110	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	689	330	110	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	689	330	110	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	943	690	230	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	997	690	230	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	940	690	230	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934647	17:7673812-7673813	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	950	690	230	S/X	agC/ag	COSV104587891,COSV53165079,COSV53562993	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	943	801	267	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	801	801	267	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	934	801	267	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	937	801	267	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	934	801	267	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1410;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	683	405	135	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	683	405	135	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=707;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1297;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	537	405	135	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	683	405	135	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=398;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=435;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=232;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1343;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1051	684	228	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	934	684	228	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	683	324	108	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	683	324	108	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	683	324	108	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	937	684	228	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	991	684	228	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	934	684	228	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1068801	17:7673818-7673819	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	944	684	228	R/X	cgG/cg	COSV52712702,COSV53164528,COSV53387047	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	943-944	801-802	267-268	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	801-802	801-802	267-268	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597362206,COSV53618401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	934-935	801-802	267-268	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	937-938	801-802	267-268	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	934-935	801-802	267-268	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362206,COSV53618401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1410;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	683-684	405-406	135-136	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	683-684	405-406	135-136	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362206,COSV53618401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=707;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362206,COSV53618401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1297;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	537-538	405-406	135-136	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	683-684	405-406	135-136	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362206,COSV53618401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=398;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362206,COSV53618401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=435;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597362206,COSV53618401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=231;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362206,COSV53618401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1343;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1051-1052	684-685	228-229	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	934-935	684-685	228-229	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	683-684	324-325	108-109	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	683-684	324-325	108-109	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	683-684	324-325	108-109	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	937-938	684-685	228-229	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	991-992	684-685	228-229	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	934-935	684-685	228-229	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
640648	17:7673818-7673818	C	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	944-945	684-685	228-229	-/X	-/G	rs1597362206,COSV53618401	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	941	799	267	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	799	799	267	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	932	799	267	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	935	799	267	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	932	799	267	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1408;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	681	403	135	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	681	403	135	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=705;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1295;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	535	403	135	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	681	403	135	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=396;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=433;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=234;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1341;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1049	682	228	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	932	682	228	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	681	322	108	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	681	322	108	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	681	322	108	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	935	682	228	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	989	682	228	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	932	682	228	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1761541	17:7673821-7673821	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	942	682	228	R/G	Cgg/Ggg	CM120851,COSV52678166,COSV52736883,COSV52827473	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	939	797	266	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	797	797	266	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	930	797	266	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	933	797	266	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	930	797	266	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1406;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	679	401	134	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	679	401	134	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=703;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1293;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	533	401	134	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	679	401	134	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=394;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=431;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=236;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1339;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1047	680	227	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	930	680	227	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	679	320	107	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	679	320	107	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	679	320	107	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	933	680	227	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	987	680	227	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	930	680	227	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634776	17:7673822-7673823	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	940	680	227	G/X	gGa/ga	rs1567548223,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	939	797	266	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	797	797	266	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	930	797	266	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	933	797	266	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	930	797	266	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1406;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	679	401	134	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	679	401	134	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=703;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1293;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	533	401	134	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	679	401	134	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=394;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=431;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=236;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1339;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1047	680	227	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	930	680	227	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	679	320	107	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	679	320	107	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	679	320	107	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	933	680	227	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	987	680	227	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	930	680	227	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
161516	17:7673823-7673823	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	940	680	227	G/E	gGa/gAa	rs193920774,CM1414506,COSV52664019,COSV52666760,COSV53585299	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic/likely_pathogenic,pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	938	796	266	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	796	796	266	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	929	796	266	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	932	796	266	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	929	796	266	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1405;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	678	400	134	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	678	400	134	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=702;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1292;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	532	400	134	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	678	400	134	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=393;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=430;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=237;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1338;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1046	679	227	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	929	679	227	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	678	319	107	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	678	319	107	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	678	319	107	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	932	679	227	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	986	679	227	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	929	679	227	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376605	17:7673824-7673824	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	939	679	227	G/R	Gga/Cga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	938	796	266	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	796	796	266	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	929	796	266	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	932	796	266	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	929	796	266	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1405;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	678	400	134	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	678	400	134	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=702;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1292;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	532	400	134	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	678	400	134	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=393;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=430;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=237;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1338;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1046	679	227	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	929	679	227	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	678	319	107	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	678	319	107	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	678	319	107	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	932	679	227	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	986	679	227	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	929	679	227	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458566	17:7673824-7673824	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	939	679	227	G/R	Gga/Aga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	937-938	795-796	265-266	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	795-796	795-796	265-266	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525344,COSV105023136,COSV52778488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	928-929	795-796	265-266	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	931-932	795-796	265-266	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	928-929	795-796	265-266	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525344,COSV105023136,COSV52778488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1404;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	677-678	399-400	133-134	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	677-678	399-400	133-134	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525344,COSV105023136,COSV52778488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=701;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525344,COSV105023136,COSV52778488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1291;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	531-532	399-400	133-134	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	677-678	399-400	133-134	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525344,COSV105023136,COSV52778488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=392;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525344,COSV105023136,COSV52778488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=429;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525344,COSV105023136,COSV52778488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=237;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525344,COSV105023136,COSV52778488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1337;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1045-1046	678-679	226-227	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	928-929	678-679	226-227	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	677-678	318-319	106-107	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	677-678	318-319	106-107	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	677-678	318-319	106-107	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	931-932	678-679	226-227	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	985-986	678-679	226-227	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	928-929	678-679	226-227	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
492623	17:7673824-7673825	AG	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	938-939	678-679	226-227	LG/L*	ctGGga/ctCTga	rs1555525344,COSV105023136,COSV52778488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	938	796	266	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	796	796	266	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	929	796	266	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	932	796	266	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	929	796	266	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1405;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	678	400	134	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	678	400	134	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=702;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1292;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	532	400	134	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	678	400	134	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=393;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=430;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=237;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1338;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1046	679	227	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	929	679	227	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	678	319	107	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	678	319	107	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	678	319	107	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	932	679	227	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	986	679	227	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	929	679	227	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
954591	17:7673824-7673824	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	939	679	227	G/*	Gga/Tga	rs1057519990,COSV52670619,COSV52672762,COSV52751844	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-934	?-792	?-264	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-792	?-792	?-264	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-925	?-792	?-264	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-928	?-792	?-264	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-925	?-792	?-264	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1388;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-674	?-396	?-132	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-674	?-396	?-132	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=685;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1275;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-528	?-396	?-132	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-674	?-396	?-132	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=376;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=413;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=241;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1321;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-1042	?-675	?-225	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-925	?-675	?-225	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-674	?-315	?-105	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-674	?-315	?-105	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-674	?-315	?-105	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-928	?-675	?-225	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-982	?-675	?-225	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-925	?-675	?-225	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760818	17:7673827-7673841	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant,NMD_transcript_variant	?-935	?-675	?-225	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	933	791	264	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	791	791	264	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	924	791	264	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	927	791	264	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	924	791	264	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1400;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	673	395	132	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	673	395	132	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=697;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1287;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	527	395	132	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	673	395	132	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=388;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=425;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=242;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1333;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1041	674	225	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	924	674	225	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	673	314	105	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	673	314	105	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	673	314	105	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	927	674	225	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	981	674	225	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	924	674	225	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1457593	17:7673828-7673829	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	934	674	225	L/X	cTa/ca	COSV104369527,COSV52672465,COSV52890118,COSV53470181	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	932	790	264	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	790	790	264	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	923	790	264	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	926	790	264	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	923	790	264	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1399;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	672	394	132	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	672	394	132	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1286;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	526	394	132	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	672	394	132	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=387;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=424;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=243;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1332;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1040	673	225	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	923	673	225	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	672	313	105	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	672	313	105	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	672	313	105	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	926	673	225	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	980	673	225	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	923	673	225	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406573	17:7673829-7673830	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	933	673	225	L/X	Cta/ta	rs1060501194,COSV52688526,COSV52700343,COSV53038101,COSV53098291	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	930	788	263	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	788	788	263	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597362423,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	921	788	263	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	924	788	263	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	921	788	263	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362423,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1397;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	670	392	131	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	670	392	131	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362423,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=694;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362423,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1284;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	524	392	131	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	670	392	131	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362423,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=385;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362423,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=422;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597362423,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=245;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362423,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1330;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1038	671	224	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	921	671	224	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	670	311	104	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	670	311	104	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	670	311	104	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	924	671	224	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	978	671	224	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	921	671	224	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
643332	17:7673831-7673832	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	931	671	224	N/X	aAt/at	rs1597362423,COSV53208998	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	928	786	262	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	786	786	262	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52782687,COSV53005312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	919	786	262	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	922	786	262	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	919	786	262	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52782687,COSV53005312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1395;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	668	390	130	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	668	390	130	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52782687,COSV53005312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=692;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52782687,COSV53005312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1282;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	522	390	130	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	668	390	130	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52782687,COSV53005312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=383;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52782687,COSV53005312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=420;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52782687,COSV53005312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=247;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52782687,COSV53005312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1328;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1036	669	223	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	919	669	223	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	668	309	103	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	668	309	103	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	668	309	103	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	922	669	223	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	976	669	223	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	919	669	223	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1459624	17:7673833-7673834	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	929	669	223	G/X	ggT/gg	COSV52782687,COSV53005312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant,splice_region_variant	927	785	262	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant,splice_region_variant	785	785	262	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs879253905,COSV52677105,COSV52952688	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant,splice_region_variant	918	785	262	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant,splice_region_variant	921	785	262	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant,splice_region_variant	918	785	262	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253905,COSV52677105,COSV52952688	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1394;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant,splice_region_variant	667	389	130	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant,splice_region_variant	667	389	130	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253905,COSV52677105,COSV52952688	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=691;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253905,COSV52677105,COSV52952688	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1281;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant,splice_region_variant	521	389	130	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant,splice_region_variant	667	389	130	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253905,COSV52677105,COSV52952688	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=382;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253905,COSV52677105,COSV52952688	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=419;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs879253905,COSV52677105,COSV52952688	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=248;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253905,COSV52677105,COSV52952688	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1327;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant,splice_region_variant	1035	668	223	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant,splice_region_variant	918	668	223	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant,splice_region_variant	667	308	103	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant,splice_region_variant	667	308	103	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant,splice_region_variant	667	308	103	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant,splice_region_variant	921	668	223	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant,splice_region_variant	975	668	223	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant,splice_region_variant	918	668	223	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
245698	17:7673834-7673835	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,splice_region_variant,NMD_transcript_variant	928	668	223	G/X	gGt/gt	rs879253905,COSV52677105,COSV52952688	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1391;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1278;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=379;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=416;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=251;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1324;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458565	17:7673838-7673838	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1391;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1278;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=379;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=416;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=251;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1324;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634661	17:7673838-7673838	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525367,CS137625,COSV52668714,COSV52729930,COSV53769335	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1390;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=687;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1277;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=378;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=415;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=252;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1323;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406603	17:7673839-7673839	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1390;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=687;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1277;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=378;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=415;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=252;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1323;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635385	17:7673839-7673839	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1390;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=687;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1277;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=378;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=415;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=252;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1323;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635386	17:7673839-7673839	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs1060501207,CS169322,COSV52818160,COSV52984227,COSV53085853	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1069;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=366;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=956;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=57;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=94;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=572;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1002;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634709	17:7674159-7674159	GGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCAT	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567548789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	923-?	781-?	261-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	781-?	781-?	261-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	781-?	781-?	261-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	914-?	781-?	261-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	917-?	781-?	261-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	914-?	781-?	261-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1047;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	663-?	385-?	129-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	663-?	385-?	129-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=344;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=934;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	517-?	385-?	129-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	663-?	385-?	129-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=35;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=72;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=586;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=980;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	1031-?	664-?	222-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	914-?	664-?	222-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	663-?	304-?	102-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	663-?	304-?	102-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	663-?	304-?	102-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	917-?	664-?	222-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	971-?	664-?	222-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	914-?	664-?	222-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1760741	17:7674172-7674182	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant,NMD_transcript_variant	924-?	664-?	222-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548832	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1050;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548832	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=347;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548832	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=937;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548832	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=38;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548832	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=75;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567548832	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548832	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=983;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
579855	17:7674174-7674179	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567548832	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1050;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=347;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=937;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=38;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=75;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=592;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=983;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231294	17:7674179-7674179	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs876659076,COSV52817854,COSV52933377,COSV53031948	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1049;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=346;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=936;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=37;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=74;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=593;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
496048	17:7674180-7674180	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1049;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=346;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=936;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=37;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=74;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=593;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634684	17:7674180-7674180	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525429,COSV52665287,COSV52673806,COSV52698978	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	914	772	258	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	772	772	258	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	772	772	258	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	905	772	258	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	908	772	258	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	905	772	258	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1038;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	654	376	126	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	654	376	126	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=335;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=925;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	508	376	126	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	654	376	126	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=26;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=63;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	1022	655	219	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	905	655	219	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	654	295	99	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	654	295	99	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	654	295	99	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	908	655	219	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	962	655	219	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	905	655	219	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
486557	17:7674191-7674191	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	915	655	219	E/*	Gaa/Taa	rs121912652,CM900213,COSV52684909,COSV52740428,COSV52828352	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	910-911	768-769	256-257	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	768-769	768-769	256-257	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	768-769	768-769	256-257	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	901-902	768-769	256-257	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	904-905	768-769	256-257	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	901-902	768-769	256-257	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1034;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	650-651	372-373	124-125	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	650-651	372-373	124-125	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=331;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=921;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	504-505	372-373	124-125	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	650-651	372-373	124-125	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=22;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=59;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=607;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=967;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1018-1019	651-652	217-218	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	901-902	651-652	217-218	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	650-651	291-292	97-98	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	650-651	291-292	97-98	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	650-651	291-292	97-98	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	904-905	651-652	217-218	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	958-959	651-652	217-218	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	901-902	651-652	217-218	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1400613	17:7674193-7674195	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	911-912	651-652	217-218	TL/TX	acACtg/actg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	908-912	766-770	256-257	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	766-770	766-770	256-257	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	766-770	766-770	256-257	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	899-903	766-770	256-257	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	902-906	766-770	256-257	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	899-903	766-770	256-257	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1032;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	648-652	370-374	124-125	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	648-652	370-374	124-125	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=329;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=919;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	502-506	370-374	124-125	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	648-652	370-374	124-125	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=20;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=57;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=965;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1016-1020	649-653	217-218	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	899-903	649-653	217-218	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	648-652	289-293	97-98	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	648-652	289-293	97-98	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	648-652	289-293	97-98	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	902-906	649-653	217-218	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	956-960	649-653	217-218	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	899-903	649-653	217-218	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
231331	17:7674193-7674197	TGGATGTCCTGACCTG	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	909-913	649-653	217-218	TL/QVRTSX	ACACTg/CAGGTCAGGACATCCAg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	906-908	764-766	255-256	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	764-766	764-766	255-256	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	764-766	764-766	255-256	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	897-899	764-766	255-256	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	900-902	764-766	255-256	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	897-899	764-766	255-256	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064794309	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	646-648	368-370	123-124	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	646-648	368-370	123-124	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064794309	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=327;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064794309	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=917;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	500-502	368-370	123-124	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	646-648	368-370	123-124	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064794309	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=18;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064794309	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=55;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064794309	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=610;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064794309	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=963;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	1014-1016	647-649	216-217	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	897-899	647-649	216-217	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000610623.4	Transcript	inframe_deletion	646-648	287-289	96-97	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000618944.4	Transcript	inframe_deletion	646-648	287-289	96-97	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000619186.4	Transcript	inframe_deletion	646-648	287-289	96-97	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	900-902	647-649	216-217	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	954-956	647-649	216-217	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	897-899	647-649	216-217	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420134	17:7674196-7674199	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	907-909	647-649	216-217	IT/T	aTCAca/aca	rs1064794309	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	908-909	766-767	256	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	766-767	766-767	256	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	766-767	766-767	256	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	899-900	766-767	256	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	902-903	766-767	256	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	899-900	766-767	256	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364034,COSV105016281	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1032;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	648-649	370-371	124	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	648-649	370-371	124	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364034,COSV105016281	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=329;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364034,COSV105016281	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=919;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	502-503	370-371	124	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	648-649	370-371	124	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364034,COSV105016281	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=20;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364034,COSV105016281	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=57;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597364034,COSV105016281	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364034,COSV105016281	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=965;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1016-1017	649-650	217	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	899-900	649-650	217	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	648-649	289-290	97	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	648-649	289-290	97	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	648-649	289-290	97	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	902-903	649-650	217	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	956-957	649-650	217	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	899-900	649-650	217	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
663253	17:7674196-7674196	T	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	909-910	649-650	217	T/NX	aca/aAca	rs1597364034,COSV105016281	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	903	761	254	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	761	761	254	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	761	761	254	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	894	761	254	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	897	761	254	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	894	761	254	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1027;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	643	365	122	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	643	365	122	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=324;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=914;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	497	365	122	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	643	365	122	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=15;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=52;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=960;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1011	644	215	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	894	644	215	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	643	284	95	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	643	284	95	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	643	284	95	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	897	644	215	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	951	644	215	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	894	644	215	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759844	17:7674202-7674202	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	904	644	215	I/T	aTc/aCc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	903	761	254	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	761	761	254	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	761	761	254	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	894	761	254	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	897	761	254	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	894	761	254	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1027;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	643	365	122	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	643	365	122	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=324;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=914;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	497	365	122	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	643	365	122	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=15;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=52;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=960;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1011	644	215	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	894	644	215	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	643	284	95	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	643	284	95	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	643	284	95	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	897	644	215	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	951	644	215	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	894	644	215	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
856299	17:7674202-7674202	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	904	644	215	I/N	aTc/aAc	CM151471,COSV52674699,COSV52714188,COSV52767322	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	901	759	253	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	759	759	253	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	759	759	253	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	892	759	253	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	895	759	253	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	892	759	253	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549129,COSV52677640	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1025;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	641	363	121	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	641	363	121	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549129,COSV52677640	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=322;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549129,COSV52677640	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=912;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	495	363	121	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	641	363	121	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549129,COSV52677640	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=13;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549129,COSV52677640	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=50;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567549129,COSV52677640	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=617;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549129,COSV52677640	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=958;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1009	642	214	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	892	642	214	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	641	282	94	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	641	282	94	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	641	282	94	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	895	642	214	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	949	642	214	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	892	642	214	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634788	17:7674203-7674204	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	902	642	214	T/X	acC/ac	rs1567549129,COSV52677640	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	899-900	757-758	253	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	757-758	757-758	253	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	757-758	757-758	253	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	890-891	757-758	253	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	893-894	757-758	253	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	890-891	757-758	253	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1023;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	639-640	361-362	121	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	639-640	361-362	121	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=320;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=910;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	493-494	361-362	121	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	639-640	361-362	121	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=11;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=48;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=618;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=956;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1007-1008	640-641	214	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	890-891	640-641	214	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	639-640	280-281	94	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	639-640	280-281	94	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	639-640	280-281	94	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	893-894	640-641	214	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	947-948	640-641	214	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	890-891	640-641	214	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1759609	17:7674205-7674205	T	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	900-901	640-641	214	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	899	757	253	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	757	757	253	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	757	757	253	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	890	757	253	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	893	757	253	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	890	757	253	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1023;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	639	361	121	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	639	361	121	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=320;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=910;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	493	361	121	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	639	361	121	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=11;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=48;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=619;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=956;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1007	640	214	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	890	640	214	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	639	280	94	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	639	280	94	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	639	280	94	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	893	640	214	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	947	640	214	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	890	640	214	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827132	17:7674206-7674206	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	900	640	214	T/A	Acc/Gcc	rs1597364185,COSV52783299,COSV52873550,COSV52906834	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	896	754	252	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	754	754	252	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	754	754	252	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	887	754	252	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	890	754	252	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	887	754	252	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525470,COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1020;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	636	358	120	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	636	358	120	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525470,COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=317;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525470,COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=907;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	490	358	120	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	636	358	120	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525470,COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=8;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525470,COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=45;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525470,COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=622;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525470,COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=953;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1004	637	213	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	887	637	213	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	636	277	93	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	636	277	93	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	636	277	93	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	890	637	213	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	944	637	213	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	887	637	213	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
485036	17:7674208-7674209	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	897	637	213	L/X	Ctc/tc	rs1555525470,COSV52730003	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	894	752	251	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	752	752	251	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	752	752	251	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	885	752	251	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	888	752	251	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	885	752	251	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1018;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	634	356	119	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	634	356	119	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=315;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	488	356	119	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	634	356	119	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=43;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=624;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=951;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1002	635	212	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	885	635	212	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	634	275	92	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	634	275	92	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	634	275	92	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	888	635	212	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	942	635	212	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	885	635	212	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759367	17:7674210-7674211	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	895	635	212	I/X	aTc/ac	COSV52728902,COSV52741592,COSV52816233,COSV53108676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	893	751	251	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	751	751	251	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	751	751	251	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	884	751	251	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	887	751	251	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	884	751	251	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1017;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	633	355	119	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	633	355	119	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=314;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	487	355	119	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	633	355	119	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=42;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=625;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=950;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1001	634	212	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	884	634	212	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	633	274	92	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	633	274	92	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	633	274	92	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	887	634	212	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	941	634	212	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	884	634	212	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1518844	17:7674212-7674212	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	894	634	212	I/F	Atc/Ttc	CM114005,COSV52677403,COSV52702261,COSV52772679,COSV52927118	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	892	750	250	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	750	750	250	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	750	750	250	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	883	750	250	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	886	750	250	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	883	750	250	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549203,COSV52876092	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1016;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	632	354	118	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	632	354	118	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549203,COSV52876092	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=313;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549203,COSV52876092	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=903;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	486	354	118	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	632	354	118	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549203,COSV52876092	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549203,COSV52876092	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=41;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567549203,COSV52876092	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549203,COSV52876092	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=949;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	1000	633	211	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	883	633	211	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	632	273	91	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	632	273	91	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	632	273	91	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	886	633	211	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	940	633	211	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	883	633	211	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634710	17:7674212-7674213	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	893	633	211	P/X	ccC/cc	rs1567549203,COSV52876092	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	890-891	748-749	250	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	748-749	748-749	250	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	748-749	748-749	250	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	881-882	748-749	250	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	884-885	748-749	250	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	881-882	748-749	250	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1014;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	630-631	352-353	118	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	630-631	352-353	118	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=311;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=901;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	484-485	352-353	118	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	630-631	352-353	118	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=39;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=627;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=947;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	998-999	631-632	211	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	881-882	631-632	211	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	630-631	271-272	91	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	630-631	271-272	91	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	630-631	271-272	91	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	884-885	631-632	211	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	938-939	631-632	211	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	881-882	631-632	211	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073015	17:7674214-7674214	TGAGGATGGTGAGGAT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	891-892	631-632	211	P/HPHHPHX	ccc/cATCCTCACCATCCTCAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	888	746	249	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	746	746	249	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	746	746	249	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	879	746	249	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	882	746	249	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	879	746	249	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1012;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	628	350	117	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	628	350	117	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=309;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=899;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	482	350	117	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	628	350	117	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000514944.5	Transcript	incomplete_terminal_codon_variant,coding_sequence_variant	546	467	156	X	aG/aC	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=37;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=630;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=945;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	996	629	210	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	879	629	210	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	628	269	90	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	628	269	90	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	628	269	90	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	882	629	210	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	936	629	210	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	879	629	210	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376015	17:7674217-7674217	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	889	629	210	R/T	aGg/aCg	rs587782329,COSV52666526,COSV52668050,COSV52697169,COSV52713804	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	872-886	730-744	244-248	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	730-744	730-744	244-248	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	730-744	730-744	244-248	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	863-877	730-744	244-248	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	866-880	730-744	244-248	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	863-877	730-744	244-248	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525486	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=996;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	612-626	334-348	112-116	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	612-626	334-348	112-116	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525486	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=293;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525486	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=883;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	466-480	334-348	112-116	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	612-626	334-348	112-116	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000514944.5	Transcript	inframe_deletion	530-544	451-465	151-155	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525486	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=21;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525486	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=632;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525486	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=929;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	980-994	613-627	205-209	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	863-877	613-627	205-209	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000610623.4	Transcript	inframe_deletion	612-626	253-267	85-89	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000618944.4	Transcript	inframe_deletion	612-626	253-267	85-89	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000619186.4	Transcript	inframe_deletion	612-626	253-267	85-89	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	866-880	613-627	205-209	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	920-934	613-627	205-209	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	863-877	613-627	205-209	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428865	17:7674218-7674233	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	873-887	613-627	205-209	GGMNR/-	GGCGGCATGAACCGG/-	rs1555525486	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	884	742	248	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	742	742	248	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	742	742	248	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	875	742	248	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	878	742	248	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	875	742	248	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1008;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	624	346	116	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	624	346	116	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=305;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	478	346	116	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	624	346	116	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	542	463	155	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=33;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=634;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=941;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	992	625	209	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	875	625	209	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	624	265	89	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	624	265	89	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	624	265	89	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	878	625	209	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	932	625	209	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	875	625	209	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376652	17:7674221-7674221	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	885	625	209	R/G	Cgg/Ggg	rs121912651,CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	883-884	741-742	247-248	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	741-742	741-742	247-248	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	741-742	741-742	247-248	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	874-875	741-742	247-248	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	877-878	741-742	247-248	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	874-875	741-742	247-248	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1007;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	623-624	345-346	115-116	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	623-624	345-346	115-116	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=304;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=894;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	477-478	345-346	115-116	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	623-624	345-346	115-116	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	541-542	462-463	154-155	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=32;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=634;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=940;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	991-992	624-625	208-209	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	874-875	624-625	208-209	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	623-624	264-265	88-89	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	623-624	264-265	88-89	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	623-624	264-265	88-89	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	877-878	624-625	208-209	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	931-932	624-625	208-209	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	874-875	624-625	208-209	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
437017	17:7674221-7674222	AA	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	884-885	624-625	208-209	NR/NW	aaCCgg/aaTTgg	rs1555525498,COSV52752087,COSV52979949	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	854-880	712-738	238-246	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	712-738	712-738	238-246	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	712-738	712-738	238-246	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	845-871	712-738	238-246	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	848-874	712-738	238-246	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	845-871	712-738	238-246	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=978;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	594-620	316-342	106-114	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	594-620	316-342	106-114	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=275;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=865;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	448-474	316-342	106-114	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	594-620	316-342	106-114	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000514944.5	Transcript	inframe_deletion	512-538	433-459	145-153	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567549353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=638;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=911;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	962-988	595-621	199-207	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	845-871	595-621	199-207	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000610623.4	Transcript	inframe_deletion	594-620	235-261	79-87	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000618944.4	Transcript	inframe_deletion	594-620	235-261	79-87	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000619186.4	Transcript	inframe_deletion	594-620	235-261	79-87	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	848-874	595-621	199-207	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	902-928	595-621	199-207	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	845-871	595-621	199-207	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634673	17:7674224-7674251	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	855-881	595-621	199-207	CNSSCMGGM/-	TGTAACAGTTCCTGCATGGGCGGCATG/-	rs1567549353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	880	738	246	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	738	738	246	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	738	738	246	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	871	738	246	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	874	738	246	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	871	738	246	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1004;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	620	342	114	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	620	342	114	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=301;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=891;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	474	342	114	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	620	342	114	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	538	459	153	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=29;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=638;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=937;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	988	621	207	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	871	621	207	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	620	261	87	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	620	261	87	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	620	261	87	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	874	621	207	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	928	621	207	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	871	621	207	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758655	17:7674225-7674225	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	881	621	207	M/I	atG/atC	COSV52735934,COSV52772732,COSV53038458,COSV53481758	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	858-878	716-736	239-246	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	716-736	716-736	239-246	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	716-736	716-736	239-246	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	849-869	716-736	239-246	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	852-872	716-736	239-246	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	849-869	716-736	239-246	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	598-618	320-340	107-114	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	598-618	320-340	107-114	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=279;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=869;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	452-472	320-340	107-114	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	598-618	320-340	107-114	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000514944.5	Transcript	inframe_deletion	516-536	437-457	146-153	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=640;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=915;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	966-986	599-619	200-207	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	849-869	599-619	200-207	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000610623.4	Transcript	inframe_deletion	598-618	239-259	80-87	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000618944.4	Transcript	inframe_deletion	598-618	239-259	80-87	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000619186.4	Transcript	inframe_deletion	598-618	239-259	80-87	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	852-872	599-619	200-207	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	906-926	599-619	200-207	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	849-869	599-619	200-207	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
231606	17:7674226-7674247	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	859-879	599-619	200-207	NSSCMGGM/M	aACAGTTCCTGCATGGGCGGCAtg/atg	rs876659260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	879	737	246	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	737	737	246	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	737	737	246	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	870	737	246	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	873	737	246	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	870	737	246	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1003;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	619	341	114	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	619	341	114	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=300;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=890;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	473	341	114	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	619	341	114	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	537	458	153	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=28;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=936;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	987	620	207	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	870	620	207	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	619	260	87	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	619	260	87	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	619	260	87	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	873	620	207	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	927	620	207	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	870	620	207	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480764	17:7674226-7674226	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	880	620	207	M/K	aTg/aAg	rs587780074,CM157012,COSV52668375,COSV52693504,COSV52778210	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	876-877	734-735	245	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	734-735	734-735	245	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	734-735	734-735	245	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	867-868	734-735	245	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	870-871	734-735	245	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	867-868	734-735	245	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52700518,COSV53649292	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1000;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	616-617	338-339	113	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	616-617	338-339	113	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52700518,COSV53649292	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=297;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52700518,COSV53649292	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	470-471	338-339	113	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	616-617	338-339	113	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	534-535	455-456	152	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52700518,COSV53649292	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=25;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52700518,COSV53649292	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=641;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52700518,COSV53649292	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=933;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	984-985	617-618	206	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	867-868	617-618	206	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	616-617	257-258	86	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	616-617	257-258	86	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	616-617	257-258	86	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	870-871	617-618	206	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	924-925	617-618	206	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	867-868	617-618	206	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
861760	17:7674228-7674229	AT	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	877-878	617-618	206	G/D	gGC/gAT	COSV52700518,COSV53649292	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	876	734	245	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	734	734	245	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	734	734	245	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	867	734	245	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	870	734	245	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	867	734	245	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1000;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	616	338	113	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	616	338	113	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=297;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	470	338	113	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	616	338	113	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	534	455	152	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=25;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=642;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=933;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	984	617	206	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	867	617	206	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	616	257	86	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	616	257	86	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	616	257	86	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	870	617	206	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	924	617	206	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	867	617	206	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376603	17:7674229-7674229	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	877	617	206	G/V	gGc/gTc	rs121912656,CM010464,CM900209,COSV52666323,COSV52667838,COSV52745465	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	873	731	244	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	731	731	244	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	731	731	244	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	864	731	244	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	867	731	244	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	864	731	244	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=997;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	613	335	112	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	613	335	112	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=294;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=884;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	467	335	112	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	613	335	112	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	531	452	151	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=22;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=645;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=930;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	981	614	205	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	864	614	205	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	613	254	85	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	613	254	85	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	613	254	85	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	867	614	205	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	921	614	205	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	864	614	205	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1050359	17:7674231-7674232	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	874	614	205	G/X	gGc/gc	CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	873	731	244	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	731	731	244	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	731	731	244	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	864	731	244	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	867	731	244	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	864	731	244	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=997;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	613	335	112	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	613	335	112	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=294;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=884;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	467	335	112	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	613	335	112	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	531	452	151	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=22;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=645;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=930;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	981	614	205	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	864	614	205	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	613	254	85	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	613	254	85	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	613	254	85	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	867	614	205	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	921	614	205	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	864	614	205	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
372785	17:7674232-7674232	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	874	614	205	G/D	gGc/gAc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	873	731	244	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	731	731	244	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	731	731	244	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	864	731	244	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	867	731	244	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	864	731	244	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=997;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	613	335	112	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	613	335	112	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=294;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=884;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	467	335	112	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	613	335	112	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	531	452	151	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=22;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=645;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=930;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	981	614	205	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	864	614	205	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	613	254	85	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	613	254	85	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	613	254	85	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	867	614	205	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	921	614	205	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	864	614	205	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376601	17:7674232-7674232	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	874	614	205	G/V	gGc/gTc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	873	731	244	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	731	731	244	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	731	731	244	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	864	731	244	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	867	731	244	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	864	731	244	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=997;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	613	335	112	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	613	335	112	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=294;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=884;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	467	335	112	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	613	335	112	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	531	452	151	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=22;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=645;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=930;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	981	614	205	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	864	614	205	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	613	254	85	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	613	254	85	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	613	254	85	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	867	614	205	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	921	614	205	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	864	614	205	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458560	17:7674232-7674232	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	874	614	205	G/A	gGc/gCc	rs985033810,CM056069,CM070298,COSV52661058,COSV52724858,COSV52839584	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	872	730	244	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	730	730	244	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	730	730	244	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	863	730	244	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	866	730	244	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	863	730	244	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=996;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	612	334	112	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	612	334	112	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=293;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=883;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	466	334	112	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	612	334	112	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	530	451	151	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=21;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=646;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=929;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	980	613	205	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	863	613	205	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	612	253	85	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	612	253	85	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	612	253	85	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	866	613	205	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	920	613	205	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	863	613	205	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376600	17:7674233-7674233	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	873	613	205	G/S	Ggc/Agc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	872	730	244	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	730	730	244	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	730	730	244	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	863	730	244	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	866	730	244	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	863	730	244	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=996;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	612	334	112	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	612	334	112	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=293;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=883;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	466	334	112	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	612	334	112	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	530	451	151	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=21;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=646;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=929;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	980	613	205	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	863	613	205	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	612	253	85	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	612	253	85	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	612	253	85	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	866	613	205	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	920	613	205	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	863	613	205	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376602	17:7674233-7674233	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	873	613	205	G/R	Ggc/Cgc	rs1057519989,CM144215,COSV52668392,COSV52676997,COSV52808251	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	868-869	726-727	242-243	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	726-727	726-727	242-243	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	726-727	726-727	242-243	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	859-860	726-727	242-243	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	862-863	726-727	242-243	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	859-860	726-727	242-243	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53383240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=992;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	608-609	330-331	110-111	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	608-609	330-331	110-111	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53383240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=289;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53383240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=879;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	462-463	330-331	110-111	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	608-609	330-331	110-111	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	526-527	447-448	149-150	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53383240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=17;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53383240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=649;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53383240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=925;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	976-977	609-610	203-204	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	859-860	609-610	203-204	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	608-609	249-250	83-84	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	608-609	249-250	83-84	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	608-609	249-250	83-84	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	862-863	609-610	203-204	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	916-917	609-610	203-204	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	859-860	609-610	203-204	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1802475	17:7674235-7674237	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	869-870	609-610	203-204	CM/CX	tgCAtg/tgtg	COSV53383240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	868	726	242	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	726	726	242	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	726	726	242	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	859	726	242	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	862	726	242	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	859	726	242	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=992;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	608	330	110	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	608	330	110	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=289;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=879;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	462	330	110	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	608	330	110	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	526	447	149	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=17;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=650;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=925;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	976	609	203	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	859	609	203	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	608	249	83	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	608	249	83	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	608	249	83	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	862	609	203	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	916	609	203	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	859	609	203	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1460346	17:7674237-7674237	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	869	609	203	C/*	tgC/tgA	CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	868	726	242	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	726	726	242	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	726	726	242	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	859	726	242	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	862	726	242	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	859	726	242	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=992;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	608	330	110	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	608	330	110	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=289;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=879;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	462	330	110	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	608	330	110	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	526	447	149	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=17;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=650;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=925;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	976	609	203	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	859	609	203	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	608	249	83	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	608	249	83	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	608	249	83	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	862	609	203	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	916	609	203	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	859	609	203	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376580	17:7674237-7674237	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	869	609	203	C/W	tgC/tgG	rs375874539,CM102354,COSV52677195,COSV52704436,COSV53034631	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	857-866	715-724	239-242	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	715-724	715-724	239-242	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	715-724	715-724	239-242	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	848-857	715-724	239-242	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	851-860	715-724	239-242	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	848-857	715-724	239-242	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525518	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=981;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	597-606	319-328	107-110	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	597-606	319-328	107-110	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525518	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=278;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525518	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=868;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	451-460	319-328	107-110	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	597-606	319-328	107-110	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	515-524	436-445	146-149	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525518	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525518	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=652;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525518	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=914;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	965-974	598-607	200-203	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	848-857	598-607	200-203	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	597-606	238-247	80-83	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	597-606	238-247	80-83	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	597-606	238-247	80-83	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	851-860	598-607	200-203	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	905-914	598-607	200-203	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	848-857	598-607	200-203	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458558	17:7674238-7674248	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	858-867	598-607	200-203	NSSC/X	AACAGTTCCTgc/gc	rs1555525518	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	865	723	241	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	723	723	241	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	723	723	241	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	856	723	241	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	859	723	241	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	856	723	241	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53025058,COSV53153033,COSV53211006	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=989;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	605	327	109	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	605	327	109	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53025058,COSV53153033,COSV53211006	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=286;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53025058,COSV53153033,COSV53211006	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=876;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	459	327	109	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	605	327	109	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	523	444	148	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53025058,COSV53153033,COSV53211006	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=14;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53025058,COSV53153033,COSV53211006	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=653;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53025058,COSV53153033,COSV53211006	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=922;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	973	606	202	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	856	606	202	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	605	246	82	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	605	246	82	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	605	246	82	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	859	606	202	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	913	606	202	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	856	606	202	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1074338	17:7674239-7674240	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	866	606	202	S/X	tcC/tc	COSV53025058,COSV53153033,COSV53211006	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	858-864	716-722	239-241	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	716-722	716-722	239-241	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	716-722	716-722	239-241	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	849-855	716-722	239-241	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	852-858	716-722	239-241	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	849-855	716-722	239-241	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	598-604	320-326	107-109	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	598-604	320-326	107-109	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=279;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=869;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	452-458	320-326	107-109	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	598-604	320-326	107-109	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	516-522	437-443	146-148	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=654;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=915;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	966-972	599-605	200-202	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	849-855	599-605	200-202	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	598-604	239-245	80-82	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	598-604	239-245	80-82	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	598-604	239-245	80-82	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	852-858	599-605	200-202	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	906-912	599-605	200-202	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	849-855	599-605	200-202	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1386939	17:7674240-7674247	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	859-865	599-605	200-202	NSS/X	aACAGTTCc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	857-864	715-722	239-241	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	715-722	715-722	239-241	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	715-722	715-722	239-241	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	848-855	715-722	239-241	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	851-858	715-722	239-241	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	848-855	715-722	239-241	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53709802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=981;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	597-604	319-326	107-109	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	597-604	319-326	107-109	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53709802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=278;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53709802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=868;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	451-458	319-326	107-109	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	597-604	319-326	107-109	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	515-522	436-443	146-148	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53709802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53709802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=654;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53709802	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=914;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	965-972	598-605	200-202	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	848-855	598-605	200-202	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	597-604	238-245	80-82	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	597-604	238-245	80-82	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	597-604	238-245	80-82	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	851-858	598-605	200-202	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	905-912	598-605	200-202	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	848-855	598-605	200-202	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1757395	17:7674241-7674248	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	858-865	598-605	200-202	NSS/X	AACAGTTCc/Tc	COSV53709802	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	864	722	241	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	722	722	241	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	722	722	241	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	855	722	241	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	858	722	241	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	855	722	241	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=988;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	604	326	109	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	604	326	109	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=285;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=875;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	458	326	109	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	604	326	109	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	522	443	148	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=13;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=654;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=921;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	972	605	202	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	855	605	202	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	604	245	82	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	604	245	82	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	604	245	82	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	858	605	202	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	912	605	202	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	855	605	202	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376663	17:7674241-7674241	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	865	605	202	S/Y	tCc/tAc	rs28934573,CM1212186,CM920673,COSV52661688,COSV52662386,COSV52713934,COSV52760886	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	863	721	241	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	721	721	241	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	721	721	241	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	854	721	241	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	857	721	241	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	854	721	241	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=987;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	603	325	109	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	603	325	109	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=284;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=874;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	457	325	109	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	603	325	109	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	521	442	148	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=920;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	971	604	202	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	854	604	202	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	603	244	82	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	603	244	82	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	603	244	82	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	857	604	202	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	911	604	202	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	854	604	202	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
958618	17:7674241-7674242	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	864	604	202	S/X	Tcc/cc	CD984149,CM942121,COSV52670786,COSV52675302,COSV53004514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	862-863	720-721	240-241	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	720-721	720-721	240-241	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	720-721	720-721	240-241	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	853-854	720-721	240-241	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	856-857	720-721	240-241	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	853-854	720-721	240-241	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53678197	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=986;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	602-603	324-325	108-109	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	602-603	324-325	108-109	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53678197	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=283;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53678197	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=873;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	456-457	324-325	108-109	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	602-603	324-325	108-109	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	520-521	441-442	147-148	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53678197	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53678197	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53678197	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=919;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	970-971	603-604	201-202	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	853-854	603-604	201-202	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	602-603	243-244	81-82	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	602-603	243-244	81-82	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	602-603	243-244	81-82	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	856-857	603-604	201-202	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	910-911	603-604	201-202	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	853-854	603-604	201-202	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1414190	17:7674242-7674242	ACTGTTACACATGTAGTTGTAGTGGATGC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	863-864	603-604	201-202	-/ASTTTTCVTX	-/GCATCCACTACAACTACATGTGTAACAGT	COSV53678197	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	860	718	240	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	718	718	240	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	718	718	240	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	851	718	240	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	854	718	240	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	851	718	240	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=984;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	600	322	108	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	600	322	108	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=281;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=871;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	454	322	108	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	600	322	108	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	518	439	147	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=658;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=917;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	968	601	201	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	851	601	201	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	600	241	81	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	600	241	81	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	600	241	81	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	854	601	201	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	908	601	201	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	851	601	201	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
584921	17:7674245-7674245	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	861	601	201	S/G	Agt/Ggt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	860	718	240	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	718	718	240	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	718	718	240	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	851	718	240	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	854	718	240	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	851	718	240	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=984;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	600	322	108	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	600	322	108	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=281;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=871;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	454	322	108	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	600	322	108	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	518	439	147	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=658;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=917;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	968	601	201	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	851	601	201	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	600	241	81	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	600	241	81	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	600	241	81	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	854	601	201	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	908	601	201	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	851	601	201	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
826894	17:7674245-7674245	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	861	601	201	S/R	Agt/Cgt	rs1567549584,CM169323,COSV52677032,COSV53097438,COSV53263148,COSV53328299,COSV53415278	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	858	716	239	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	716	716	239	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	716	716	239	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	849	716	239	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	852	716	239	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	849	716	239	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	598	320	107	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	598	320	107	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=279;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=869;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	452	320	107	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	598	320	107	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	516	437	146	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=915;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	966	599	200	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	849	599	200	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	598	239	80	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	598	239	80	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	598	239	80	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	852	599	200	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	906	599	200	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	849	599	200	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406580	17:7674246-7674247	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	859	599	200	N/X	aAc/ac	rs1060501197,COSV52661127,COSV52664176,COSV52966384	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	858-859	716-717	239	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	716-717	716-717	239	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	716-717	716-717	239	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	849-850	716-717	239	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	852-853	716-717	239	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	849-850	716-717	239	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691541,COSV104583347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	598-599	320-321	107	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	598-599	320-321	107	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691541,COSV104583347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=279;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691541,COSV104583347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=869;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	452-453	320-321	107	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	598-599	320-321	107	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	516-517	437-438	146	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691541,COSV104583347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691541,COSV104583347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691541,COSV104583347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=915;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	966-967	599-600	200	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	849-850	599-600	200	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	598-599	239-240	80	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	598-599	239-240	80	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	598-599	239-240	80	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	852-853	599-600	200	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	906-907	599-600	200	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	849-850	599-600	200	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429707	17:7674246-7674246	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	859-860	599-600	200	N/NX	aac/aaTc	rs1131691541,COSV104583347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	858	716	239	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	716	716	239	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	716	716	239	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	849	716	239	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	852	716	239	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	849	716	239	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	598	320	107	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	598	320	107	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=279;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=869;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	452	320	107	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	598	320	107	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	516	437	146	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=915;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	966	599	200	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	849	599	200	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	598	239	80	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	598	239	80	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	598	239	80	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	852	599	200	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	906	599	200	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	849	599	200	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376637	17:7674247-7674247	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	859	599	200	N/S	aAc/aGc	rs1057519999,COSV52661127,COSV52664176,COSV52966384	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	856	714	238	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	714	714	238	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	714	714	238	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	847	714	238	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	850	714	238	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	847	714	238	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=980;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	596	318	106	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	596	318	106	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=277;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=867;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	450	318	106	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	596	318	106	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	514	435	145	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=662;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=913;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	964	597	199	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	847	597	199	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	596	237	79	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	596	237	79	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	596	237	79	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	850	597	199	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	904	597	199	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	847	597	199	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480748	17:7674248-7674249	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	857	597	199	C/X	tgT/tg	rs1555525537,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	855-856	713-714	238	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	713-714	713-714	238	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	713-714	713-714	238	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	846-847	713-714	238	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	849-850	713-714	238	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	846-847	713-714	238	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525539	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=979;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	595-596	317-318	106	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	595-596	317-318	106	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525539	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=276;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525539	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=866;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	449-450	317-318	106	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	595-596	317-318	106	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	513-514	434-435	145	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525539	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525539	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=662;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525539	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=912;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	963-964	596-597	199	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	846-847	596-597	199	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	595-596	236-237	79	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	595-596	236-237	79	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	595-596	236-237	79	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	849-850	596-597	199	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	903-904	596-597	199	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	846-847	596-597	199	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
480754	17:7674248-7674250	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	856-857	596-597	199	C/X	tGT/t	rs1555525539	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	844-856	702-714	234-238	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	702-714	702-714	234-238	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	702-714	702-714	234-238	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	835-847	702-714	234-238	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	838-850	702-714	234-238	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	835-847	702-714	234-238	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=968;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	584-596	306-318	102-106	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	584-596	306-318	102-106	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=265;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=855;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	438-450	306-318	102-106	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	584-596	306-318	102-106	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	502-514	423-435	141-145	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	97-?	-	-	-	-	rs1567549676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567549676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=662;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=901;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	952-964	585-597	195-199	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	835-847	585-597	195-199	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	584-596	225-237	75-79	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	584-596	225-237	75-79	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	584-596	225-237	75-79	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	838-850	585-597	195-199	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	892-904	585-597	195-199	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	835-847	585-597	195-199	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
574669	17:7674248-7674261	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	845-857	585-597	195-199	YNYMC/X	taCAACTACATGTGT/ta	rs1567549676	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	856-857	714-715	238-239	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	714-715	714-715	238-239	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	714-715	714-715	238-239	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	847-848	714-715	238-239	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	850-851	714-715	238-239	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	847-848	714-715	238-239	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549651,COSV52663173,COSV52791488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=980;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	596-597	318-319	106-107	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	596-597	318-319	106-107	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549651,COSV52663173,COSV52791488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=277;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549651,COSV52663173,COSV52791488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=867;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	450-451	318-319	106-107	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	596-597	318-319	106-107	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	514-515	435-436	145-146	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549651,COSV52663173,COSV52791488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567549651,COSV52663173,COSV52791488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567549651,COSV52663173,COSV52791488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=913;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	964-965	597-598	199-200	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	847-848	597-598	199-200	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	596-597	237-238	79-80	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	596-597	237-238	79-80	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	596-597	237-238	79-80	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	850-851	597-598	199-200	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	904-905	597-598	199-200	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	847-848	597-598	199-200	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634772	17:7674248-7674248	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	857-858	597-598	199-200	-/X	-/T	rs1567549651,COSV52663173,COSV52791488	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	856	714	238	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	714	714	238	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	714	714	238	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	847	714	238	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	850	714	238	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	847	714	238	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=980;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	596	318	106	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	596	318	106	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=277;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=867;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	450	318	106	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	596	318	106	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	514	435	145	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=662;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=913;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	964	597	199	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	847	597	199	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	596	237	79	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	596	237	79	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	596	237	79	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	850	597	199	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	904	597	199	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	847	597	199	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
161515	17:7674249-7674249	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	857	597	199	C/W	tgT/tgG	rs193920789,COSV52680696,COSV52840491,COSV53234319,COSV53865082	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	855-856	713-714	238	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	713-714	713-714	238	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	713-714	713-714	238	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	846-847	713-714	238	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	849-850	713-714	238	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	846-847	713-714	238	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365075,COSV52732694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=979;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	595-596	317-318	106	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	595-596	317-318	106	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365075,COSV52732694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=276;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365075,COSV52732694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=866;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	449-450	317-318	106	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	595-596	317-318	106	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	513-514	434-435	145	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365075,COSV52732694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597365075,COSV52732694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=662;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365075,COSV52732694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=912;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	963-964	596-597	199	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	846-847	596-597	199	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	595-596	236-237	79	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	595-596	236-237	79	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	595-596	236-237	79	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	849-850	596-597	199	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	903-904	596-597	199	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	846-847	596-597	199	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
803307	17:7674249-7674249	C	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	856-857	596-597	199	C/WX	tgt/tgGt	rs1597365075,COSV52732694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	855	713	238	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	713	713	238	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	713	713	238	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	846	713	238	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	849	713	238	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	846	713	238	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=979;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	595	317	106	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	595	317	106	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=276;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=866;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	449	317	106	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	595	317	106	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	513	434	145	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=663;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=912;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	963	596	199	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	846	596	199	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	595	236	79	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	595	236	79	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	595	236	79	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	849	596	199	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	903	596	199	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	846	596	199	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376574	17:7674250-7674250	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	856	596	199	C/F	tGt/tTt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	855	713	238	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	713	713	238	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	713	713	238	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	846	713	238	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	849	713	238	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	846	713	238	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=979;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	595	317	106	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	595	317	106	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=276;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=866;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	449	317	106	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	595	317	106	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	513	434	145	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=663;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=912;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	963	596	199	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	846	596	199	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	595	236	79	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	595	236	79	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	595	236	79	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	849	596	199	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	903	596	199	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	846	596	199	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376575	17:7674250-7674250	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	856	596	199	C/S	tGt/tCt	rs730882005,CM034930,COSV52661646,COSV52706816,COSV52804264	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	854	712	238	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	712	712	238	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	712	712	238	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	845	712	238	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	848	712	238	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	845	712	238	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=978;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	594	316	106	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	594	316	106	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=275;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=865;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	448	316	106	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	594	316	106	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	512	433	145	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=664;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=911;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	962	595	199	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	845	595	199	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	594	235	79	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	594	235	79	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	594	235	79	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	848	595	199	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	902	595	199	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	845	595	199	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376576	17:7674251-7674251	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	855	595	199	C/R	Tgt/Cgt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	854	712	238	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	712	712	238	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	712	712	238	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	845	712	238	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	848	712	238	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	845	712	238	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=978;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	594	316	106	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	594	316	106	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=275;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=865;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	448	316	106	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	594	316	106	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	512	433	145	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=664;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=911;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	962	595	199	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	845	595	199	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	594	235	79	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	594	235	79	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	594	235	79	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	848	595	199	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	902	595	199	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	845	595	199	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376577	17:7674251-7674251	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	855	595	199	C/G	Tgt/Ggt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	854	712	238	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	712	712	238	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	712	712	238	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	845	712	238	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	848	712	238	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	845	712	238	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=978;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	594	316	106	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	594	316	106	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=275;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=865;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	448	316	106	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	594	316	106	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	512	433	145	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=664;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=911;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	962	595	199	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	845	595	199	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	594	235	79	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	594	235	79	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	594	235	79	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	848	595	199	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	902	595	199	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	845	595	199	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
485039	17:7674251-7674251	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	855	595	199	C/S	Tgt/Agt	rs1057519981,CM025271,CM056070,COSV52699956,COSV52707471,COSV52711035,COSV52711932	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	853	711	237	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	711	711	237	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	711	711	237	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	844	711	237	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	847	711	237	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	844	711	237	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=977;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	593	315	105	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	593	315	105	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=274;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=864;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	447	315	105	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	593	315	105	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	511	432	144	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=665;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=910;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	961	594	198	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	844	594	198	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	593	234	78	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	593	234	78	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	593	234	78	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	847	594	198	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	901	594	198	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	844	594	198	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
663828	17:7674251-7674252	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	854	594	198	M/X	atG/at	rs1597365138,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	853	711	237	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	711	711	237	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	711	711	237	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	844	711	237	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	847	711	237	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	844	711	237	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=977;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	593	315	105	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	593	315	105	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=274;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=864;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	447	315	105	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	593	315	105	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	511	432	144	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=665;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=910;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	961	594	198	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	844	594	198	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	593	234	78	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	593	234	78	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	593	234	78	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	847	594	198	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	901	594	198	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	844	594	198	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1757269	17:7674252-7674252	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	854	594	198	M/I	atG/atC	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	853	711	237	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	711	711	237	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	711	711	237	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	844	711	237	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	847	711	237	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	844	711	237	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=977;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	593	315	105	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	593	315	105	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=274;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=864;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	447	315	105	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	593	315	105	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	511	432	144	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=665;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=910;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	961	594	198	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	844	594	198	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	593	234	78	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	593	234	78	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	593	234	78	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	847	594	198	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	901	594	198	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	844	594	198	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634770	17:7674252-7674252	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	854	594	198	M/I	atG/atT	rs587782664,CM011014,CM1516335,COSV52661887,COSV52681050,COSV52751406	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	852	710	237	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	710	710	237	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	710	710	237	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	843	710	237	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	846	710	237	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	843	710	237	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=976;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	592	314	105	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	592	314	105	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=273;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=863;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	446	314	105	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	592	314	105	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	510	431	144	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=909;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	960	593	198	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	843	593	198	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	592	233	78	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	592	233	78	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	592	233	78	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	846	593	198	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	900	593	198	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	843	593	198	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376636	17:7674253-7674253	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	853	593	198	M/K	aTg/aAg	rs765848205,COSV52682586,COSV53017093,COSV53037559,COSV53037741	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	850	708	236	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	708	708	236	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	708	708	236	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	841	708	236	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	844	708	236	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	841	708	236	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=974;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	590	312	104	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	590	312	104	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=271;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=861;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	444	312	104	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	590	312	104	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	508	429	143	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	103	-	-	-	-	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=668;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=907;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	958	591	197	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	841	591	197	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	590	231	77	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	590	231	77	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	590	231	77	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	844	591	197	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	898	591	197	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	841	591	197	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757085	17:7674254-7674255	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	851	591	197	Y/X	taC/ta	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	850	708	236	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	708	708	236	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	708	708	236	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	841	708	236	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	844	708	236	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	841	708	236	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=974;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	590	312	104	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	590	312	104	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=271;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=861;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	444	312	104	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	590	312	104	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	508	429	143	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	103	-	-	-	-	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=668;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=907;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	958	591	197	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	841	591	197	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	590	231	77	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	590	231	77	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	590	231	77	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	844	591	197	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	898	591	197	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	841	591	197	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1686269	17:7674255-7674255	C	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	851	591	197	Y/*	taC/taG	CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	832-844	690-702	230-234	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	690-702	690-702	230-234	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	690-702	690-702	230-234	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	823-835	690-702	230-234	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	826-838	690-702	230-234	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	823-835	690-702	230-234	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=956;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	572-584	294-306	98-102	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	572-584	294-306	98-102	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=253;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=843;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	426-438	294-306	98-102	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	572-584	294-306	98-102	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	490-502	411-423	137-141	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	85-97	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=674;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=889;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	940-952	573-585	191-195	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	823-835	573-585	191-195	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	572-584	213-225	71-75	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	572-584	213-225	71-75	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	572-584	213-225	71-75	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	826-838	573-585	191-195	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	880-892	573-585	191-195	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	823-835	573-585	191-195	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070690	17:7674260-7674273	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	833-845	573-585	191-195	TTIHY/X	acCACCATCCACTAC/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	844	702	234	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	702	702	234	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	702	702	234	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	835	702	234	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	838	702	234	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	835	702	234	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=968;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	584	306	102	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	584	306	102	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=265;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=855;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	438	306	102	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	584	306	102	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	502	423	141	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	97	-	-	-	-	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=674;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=901;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	952	585	195	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	835	585	195	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	584	225	75	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	584	225	75	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	584	225	75	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	838	585	195	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	892	585	195	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	835	585	195	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1069305	17:7674261-7674261	C	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	845	585	195	Y/*	taC/taG	COSV52783916,COSV52908090,COSV53020803,COSV53124617	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	842	700	234	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	700	700	234	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	700	700	234	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	833	700	234	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	836	700	234	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	833	700	234	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=966;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	582	304	102	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	582	304	102	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=263;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=853;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	436	304	102	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	582	304	102	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	500	421	141	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	95	-	-	-	-	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=676;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=899;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	950	583	195	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	833	583	195	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	582	223	75	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	582	223	75	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	582	223	75	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	836	583	195	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	890	583	195	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	833	583	195	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376691	17:7674263-7674263	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	843	583	195	Y/H	Tac/Cac	rs864622237,CM137618,COSV105025807,COSV52694920,COSV52730114,COSV52730255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	837	695	232	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	695	695	232	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	695	695	232	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	828	695	232	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	831	695	232	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	828	695	232	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=961;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	577	299	100	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	577	299	100	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=258;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=848;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	431	299	100	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	577	299	100	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	495	416	139	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	90	-	-	-	-	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=681;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=894;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	945	578	193	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	828	578	193	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	577	218	73	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	577	218	73	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	577	218	73	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	831	578	193	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	885	578	193	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	828	578	193	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634756	17:7674268-7674268	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	838	578	193	I/S	aTc/aGc	rs587781589,CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	837	695	232	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	695	695	232	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	695	695	232	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	828	695	232	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	831	695	232	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	828	695	232	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=961;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	577	299	100	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	577	299	100	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=258;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=848;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	431	299	100	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	577	299	100	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	495	416	139	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	90	-	-	-	-	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=681;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=894;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	945	578	193	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	828	578	193	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	577	218	73	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	577	218	73	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	577	218	73	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	831	578	193	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	885	578	193	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	828	578	193	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
850008	17:7674268-7674268	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	838	578	193	I/N	aTc/aAc	CM103212,COSV52661257,COSV52760307,COSV52829354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	827-834	685-692	229-231	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	685-692	685-692	229-231	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	685-692	685-692	229-231	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	818-825	685-692	229-231	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	821-828	685-692	229-231	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	818-825	685-692	229-231	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=951;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	567-574	289-296	97-99	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	567-574	289-296	97-99	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=248;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=838;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	421-428	289-296	97-99	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	567-574	289-296	97-99	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	485-492	406-413	136-138	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	80-87	-	-	-	-	rs730882016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=684;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=884;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	935-942	568-575	190-192	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	818-825	568-575	190-192	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	567-574	208-215	70-72	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	567-574	208-215	70-72	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	567-574	208-215	70-72	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	821-828	568-575	190-192	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	875-882	568-575	190-192	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	818-825	568-575	190-192	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182955	17:7674270-7674278	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	828-835	568-575	190-192	CTT/X	TGTACCACc/c	rs730882016	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	832	690	230	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	690	690	230	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	690	690	230	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	823	690	230	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	826	690	230	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	823	690	230	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CD136735,COSV53715467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=956;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	572	294	98	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	572	294	98	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD136735,COSV53715467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=253;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD136735,COSV53715467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=843;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	426	294	98	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	572	294	98	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	490	411	137	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	85	-	-	-	-	CD136735,COSV53715467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD136735,COSV53715467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=686;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD136735,COSV53715467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=889;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	940	573	191	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	823	573	191	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	572	213	71	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	572	213	71	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	572	213	71	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	826	573	191	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	880	573	191	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	823	573	191	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1076652	17:7674272-7674273	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	833	573	191	T/X	acC/ac	CD136735,COSV53715467	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	828-829	686-687	229	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	686-687	686-687	229	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	686-687	686-687	229	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	819-820	686-687	229	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	822-823	686-687	229	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	819-820	686-687	229	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=952;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	568-569	290-291	97	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	568-569	290-291	97	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=249;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=839;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	422-423	290-291	97	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	568-569	290-291	97	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	486-487	407-408	136	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	81-82	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=689;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=885;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	936-937	569-570	190	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	819-820	569-570	190	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	568-569	209-210	70	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	568-569	209-210	70	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	568-569	209-210	70	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	822-823	569-570	190	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	876-877	569-570	190	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	819-820	569-570	190	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
863486	17:7674275-7674277	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	829-830	569-570	190	C/X	tGT/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	825-826	683-684	228	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	683-684	683-684	228	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	683-684	683-684	228	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	816-817	683-684	228	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	819-820	683-684	228	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	816-817	683-684	228	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=949;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	565-566	287-288	96	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	565-566	287-288	96	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=246;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=836;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	419-420	287-288	96	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	565-566	287-288	96	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	483-484	404-405	135	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	78-79	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=692;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=882;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	933-934	566-567	189	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	816-817	566-567	189	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	565-566	206-207	69	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	565-566	206-207	69	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	565-566	206-207	69	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	819-820	566-567	189	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	873-874	566-567	189	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	816-817	566-567	189	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1382148	17:7674278-7674280	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	826-827	566-567	189	D/X	gAC/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	823-824	681-682	227-228	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	681-682	681-682	227-228	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	681-682	681-682	227-228	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	814-815	681-682	227-228	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	817-818	681-682	227-228	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	814-815	681-682	227-228	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567550002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=947;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	563-564	285-286	95-96	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	563-564	285-286	95-96	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567550002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=244;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567550002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=834;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	417-418	285-286	95-96	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	563-564	285-286	95-96	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	481-482	402-403	134-135	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	76-77	-	-	-	-	rs1567550002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567550002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=694;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567550002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=880;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	931-932	564-565	188-189	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	814-815	564-565	188-189	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	563-564	204-205	68-69	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	563-564	204-205	68-69	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	563-564	204-205	68-69	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	817-818	564-565	188-189	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	871-872	564-565	188-189	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	814-815	564-565	188-189	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634696	17:7674281-7674281	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	824-825	564-565	188-189	-/X	-/T	rs1567550002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	822	680	227	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	680	680	227	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	680	680	227	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	813	680	227	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	816	680	227	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	813	680	227	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=946;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	562	284	95	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	562	284	95	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=243;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=833;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	416	284	95	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	562	284	95	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	480	401	134	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	75	-	-	-	-	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=879;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	930	563	188	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	813	563	188	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	562	203	68	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	562	203	68	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	562	203	68	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	816	563	188	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	870	563	188	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	813	563	188	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634685	17:7674282-7674283	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	823	563	188	S/X	tCt/tt	rs1567550018,COSV52661835,COSV52739938,COSV53410104	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant,splice_region_variant	817	675	225	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant,splice_region_variant	675	675	225	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant,splice_region_variant	675	675	225	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant,splice_region_variant	808	675	225	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant,splice_region_variant	811	675	225	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant,splice_region_variant	808	675	225	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567550076,COSV52891821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=941;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant,splice_region_variant	557	279	93	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant,splice_region_variant	557	279	93	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567550076,COSV52891821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=238;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567550076,COSV52891821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=828;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant,splice_region_variant	411	279	93	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant,splice_region_variant	557	279	93	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant,splice_region_variant	475	396	132	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000574684.1	Transcript	splice_region_variant,non_coding_transcript_exon_variant	70	-	-	-	-	rs1567550076,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567550076,COSV52891821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=701;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567550076,COSV52891821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=874;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant,splice_region_variant	925	558	186	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant,splice_region_variant	808	558	186	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant,splice_region_variant	557	198	66	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant,splice_region_variant	557	198	66	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant,splice_region_variant	557	198	66	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant,splice_region_variant	811	558	186	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant,splice_region_variant	865	558	186	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant,splice_region_variant	808	558	186	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634679	17:7674287-7674288	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,splice_region_variant,NMD_transcript_variant	818	558	186	V/X	gtT/gt	rs1567550076,COSV52891821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant,splice_region_variant	815-816	673-674	225	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant,splice_region_variant	673-674	673-674	225	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant,splice_region_variant	673-674	673-674	225	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant,splice_region_variant	806-807	673-674	225	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant,splice_region_variant	809-810	673-674	225	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant,splice_region_variant	806-807	673-674	225	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=939;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant,splice_region_variant	555-556	277-278	93	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant,splice_region_variant	555-556	277-278	93	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=236;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=826;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant,splice_region_variant	409-410	277-278	93	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant,splice_region_variant	555-556	277-278	93	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant,splice_region_variant	473-474	394-395	132	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000574684.1	Transcript	splice_region_variant,non_coding_transcript_exon_variant	68-69	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=702;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=872;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant,splice_region_variant	923-924	556-557	186	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant,splice_region_variant	806-807	556-557	186	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant,splice_region_variant	555-556	196-197	66	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant,splice_region_variant	555-556	196-197	66	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant,splice_region_variant	555-556	196-197	66	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant,splice_region_variant	809-810	556-557	186	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant,splice_region_variant	863-864	556-557	186	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant,splice_region_variant	806-807	556-557	186	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454195	17:7674289-7674289	C	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,splice_region_variant,NMD_transcript_variant	816-817	556-557	186	V/GX	gtt/gGtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=938;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=235;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=825;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000574684.1	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=704;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=871;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1228368	17:7674291-7674291	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=938;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=235;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=825;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000574684.1	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=704;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=871;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
237953	17:7674291-7674291	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=938;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=235;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=825;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000574684.1	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=704;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=871;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
379336	17:7674291-7674291	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs878854073,CS011061,COSV52662773,COSV52705331,COSV52707963,COSV53154363	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=937;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=234;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=824;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000574684.1	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=705;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=870;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458555	17:7674292-7674292	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=937;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=234;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=824;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000574684.1	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=705;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=870;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635388	17:7674292-7674292	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525585,CS109519,COSV52669186,COSV52682653,COSV52687702	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=372;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	930	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=259;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1270;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=305;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
517509	17:7674857-7674857	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525703,CS034998,CS0910926,COSV52677962,COSV52797769,COSV53179168	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=371;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	929	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=258;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1271;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=304;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634752	17:7674857-7674858	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=371;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	929	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=258;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1271;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=304;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
216078	17:7674858-7674858	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,not_provided;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=371;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	929	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=258;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1271;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=304;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
630765	17:7674858-7674858	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs863224499,CS071266,CS123101,COSV52670407,COSV52712339,COSV52751788	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	814	672	224	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,synonymous_variant	672	672	224	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,synonymous_variant	672	672	224	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,synonymous_variant	805	672	224	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	808	672	224	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,synonymous_variant	805	672	224	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=370;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,synonymous_variant	554	276	92	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,synonymous_variant	554	276	92	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	928	-	-	-	-	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=257;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,synonymous_variant	408	276	92	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,synonymous_variant	554	276	92	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,synonymous_variant	472	393	131	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1272;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=303;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,synonymous_variant	922	555	185	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,synonymous_variant	805	555	185	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,synonymous_variant	554	195	65	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,synonymous_variant	554	195	65	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,synonymous_variant	554	195	65	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,synonymous_variant	808	555	185	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,synonymous_variant	862	555	185	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,synonymous_variant	805	555	185	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
80709	17:7674859-7674859	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,synonymous_variant,NMD_transcript_variant	815	555	185	E	gaG/gaA	rs267605076,CS100446,CS175905,COSV105016529,COSV52678333,COSV52681634,COSV52721244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant,splice_region_variant	797-812	655-670	219-224	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant,splice_region_variant	655-670	655-670	219-224	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant,splice_region_variant	655-670	655-670	219-224	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant,splice_region_variant	788-803	655-670	219-224	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant,splice_region_variant	791-806	655-670	219-224	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant,splice_region_variant	788-803	655-670	219-224	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525710	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=353;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant,splice_region_variant	537-552	259-274	87-92	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant,splice_region_variant	537-552	259-274	87-92	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	911-926	-	-	-	-	rs1555525710	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525710	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=240;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant,splice_region_variant	391-406	259-274	87-92	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant,splice_region_variant	537-552	259-274	87-92	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant,splice_region_variant	455-470	376-391	126-131	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525710	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525710	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1274;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525710	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=286;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant,splice_region_variant	905-920	538-553	180-185	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant,splice_region_variant	788-803	538-553	180-185	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant,splice_region_variant	537-552	178-193	60-65	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant,splice_region_variant	537-552	178-193	60-65	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant,splice_region_variant	537-552	178-193	60-65	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant,splice_region_variant	791-806	538-553	180-185	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant,splice_region_variant	845-860	538-553	180-185	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant,splice_region_variant	788-803	538-553	180-185	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
486553	17:7674860-7674876	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,splice_region_variant,NMD_transcript_variant	798-813	538-553	180-185	PYEPPE/X	CCCTATGAGCCGCCTGag/ag	rs1555525710	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	804-808	662-666	221-222	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	662-666	662-666	221-222	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	662-666	662-666	221-222	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	795-799	662-666	221-222	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	798-802	662-666	221-222	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	795-799	662-666	221-222	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=360;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	544-548	266-270	89-90	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	544-548	266-270	89-90	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	918-922	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=247;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	398-402	266-270	89-90	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	544-548	266-270	89-90	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	462-466	383-387	128-129	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1278;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=293;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	912-916	545-549	182-183	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	795-799	545-549	182-183	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	544-548	185-189	62-63	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	544-548	185-189	62-63	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	544-548	185-189	62-63	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	798-802	545-549	182-183	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	852-856	545-549	182-183	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	795-799	545-549	182-183	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1071474	17:7674864-7674869	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	805-809	545-549	182-183	EP/X	gAGCCG/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	793-808	651-666	217-222	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	651-666	651-666	217-222	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	651-666	651-666	217-222	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	784-799	651-666	217-222	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	787-802	651-666	217-222	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	784-799	651-666	217-222	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=349;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	533-548	255-270	85-90	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	533-548	255-270	85-90	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	907-922	-	-	-	-	rs786202315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=236;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	387-402	255-270	85-90	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	533-548	255-270	85-90	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	451-466	372-387	124-129	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs786202315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1278;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=282;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	901-916	534-549	178-183	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	784-799	534-549	178-183	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	533-548	174-189	58-63	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	533-548	174-189	58-63	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	533-548	174-189	58-63	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	787-802	534-549	178-183	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	841-856	534-549	178-183	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	784-799	534-549	178-183	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185612	17:7674864-7674880	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	794-809	534-549	178-183	VVPYEP/X	gtGGTGCCCTATGAGCCG/gt	rs786202315	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	807-808	665-666	222	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	665-666	665-666	222	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	665-666	665-666	222	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	798-799	665-666	222	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	801-802	665-666	222	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	798-799	665-666	222	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99435175	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=363;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	547-548	269-270	90	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	547-548	269-270	90	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	921-922	-	-	-	-	COSV99435175	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99435175	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=250;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	401-402	269-270	90	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	547-548	269-270	90	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	465-466	386-387	129	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV99435175	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99435175	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1278;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99435175	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=296;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	915-916	548-549	183	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	798-799	548-549	183	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	547-548	188-189	63	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	547-548	188-189	63	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	547-548	188-189	63	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	801-802	548-549	183	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	855-856	548-549	183	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	798-799	548-549	183	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1071812	17:7674865-7674865	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	808-809	548-549	183	P/PX	ccg/ccCg	COSV99435175	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	799-807	657-665	219-222	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	657-665	657-665	219-222	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	657-665	657-665	219-222	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	790-798	657-665	219-222	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	793-801	657-665	219-222	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	790-798	657-665	219-222	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658144	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=355;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	539-547	261-269	87-90	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	539-547	261-269	87-90	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	913-921	-	-	-	-	rs876658144	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658144	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=242;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	393-401	261-269	87-90	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	539-547	261-269	87-90	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000514944.5	Transcript	inframe_deletion	457-465	378-386	126-129	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs876658144	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658144	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1279;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658144	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=288;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	907-915	540-548	180-183	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	790-798	540-548	180-183	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000610623.4	Transcript	inframe_deletion	539-547	180-188	60-63	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000618944.4	Transcript	inframe_deletion	539-547	180-188	60-63	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000619186.4	Transcript	inframe_deletion	539-547	180-188	60-63	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	793-801	540-548	180-183	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	847-855	540-548	180-183	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	790-798	540-548	180-183	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
229689	17:7674865-7674874	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	800-808	540-548	180-183	PYEP/P	ccCTATGAGCCg/ccg	rs876658144	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	807	665	222	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	665	665	222	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	665	665	222	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	798	665	222	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	801	665	222	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	798	665	222	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=363;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	547	269	90	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	547	269	90	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	921	-	-	-	-	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=250;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	401	269	90	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	547	269	90	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	465	386	129	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1279;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=296;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	915	548	183	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	798	548	183	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	547	188	63	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	547	188	63	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	547	188	63	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	801	548	183	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	855	548	183	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	798	548	183	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634705	17:7674865-7674866	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	808	548	183	P/X	cCg/cg	rs1567551073,CM103211,COSV52774327,COSV52909202	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	804	662	221	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	662	662	221	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	662	662	221	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	795	662	221	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	798	662	221	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	795	662	221	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=360;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	544	266	89	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	544	266	89	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	918	-	-	-	-	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=247;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	398	266	89	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	544	266	89	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	462	383	128	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1282;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=293;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	912	545	182	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	795	545	182	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	544	185	62	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	544	185	62	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	544	185	62	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	798	545	182	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	852	545	182	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	795	545	182	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
237951	17:7674868-7674869	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	805	545	182	E/X	gAg/gg	rs878854071,COSV53055641,COSV53176708,COSV53268129	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	803	661	221	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	661	661	221	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	661	661	221	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	794	661	221	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	797	661	221	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	794	661	221	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=359;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	543	265	89	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	543	265	89	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	917	-	-	-	-	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=246;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	397	265	89	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	543	265	89	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	461	382	128	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1283;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=292;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	911	544	182	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	794	544	182	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	543	184	62	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	543	184	62	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	543	184	62	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	797	544	182	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	851	544	182	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	794	544	182	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634754	17:7674870-7674870	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	804	544	182	E/*	Gag/Tag	rs786201592,COSV52735606,COSV52751148,COSV52783951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	802	660	220	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	660	660	220	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	660	660	220	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	793	660	220	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	796	660	220	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	793	660	220	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=358;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	542	264	88	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	542	264	88	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	916	-	-	-	-	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=245;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	396	264	88	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	542	264	88	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	460	381	127	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1284;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=291;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	910	543	181	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	793	543	181	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	542	183	61	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	542	183	61	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	542	183	61	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	796	543	181	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	850	543	181	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	793	543	181	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634774	17:7674871-7674871	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	803	543	181	Y/*	taT/taA	rs1567551150,CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	793-800	651-658	217-220	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	651-658	651-658	217-220	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	651-658	651-658	217-220	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	784-791	651-658	217-220	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	787-794	651-658	217-220	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	784-791	651-658	217-220	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=349;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	533-540	255-262	85-88	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	533-540	255-262	85-88	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	907-914	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=236;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	387-394	255-262	85-88	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	533-540	255-262	85-88	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	451-458	372-379	124-127	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1286;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=282;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	901-908	534-541	178-181	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	784-791	534-541	178-181	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	533-540	174-181	58-61	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	533-540	174-181	58-61	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	533-540	174-181	58-61	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	787-794	534-541	178-181	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	841-848	534-541	178-181	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	784-791	534-541	178-181	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1455049	17:7674872-7674880	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	794-801	534-541	178-181	VVPY/VX	gtGGTGCCCTat/gtat	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	800	658	220	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	658	658	220	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	658	658	220	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	791	658	220	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	794	658	220	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	791	658	220	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=356;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	540	262	88	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	540	262	88	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	914	-	-	-	-	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=243;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	394	262	88	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	540	262	88	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	458	379	127	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1286;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=289;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	908	541	181	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	791	541	181	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	540	181	61	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	540	181	61	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	540	181	61	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	794	541	181	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	848	541	181	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	791	541	181	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376687	17:7674873-7674873	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	801	541	181	Y/H	Tat/Cat	rs530941076,COSV52691656,COSV52700454,COSV52760651,COSV53630086	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	794-796	652-654	218	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	652-654	652-654	218	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	652-654	652-654	218	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	785-787	652-654	218	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	788-790	652-654	218	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	785-787	652-654	218	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597367938	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=350;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	534-536	256-258	86	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	534-536	256-258	86	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	908-910	-	-	-	-	rs1597367938	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597367938	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=237;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	388-390	256-258	86	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	534-536	256-258	86	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000514944.5	Transcript	inframe_deletion	452-454	373-375	125	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597367938	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597367938	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1290;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597367938	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=283;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	902-904	535-537	179	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	785-787	535-537	179	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000610623.4	Transcript	inframe_deletion	534-536	175-177	59	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000618944.4	Transcript	inframe_deletion	534-536	175-177	59	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000619186.4	Transcript	inframe_deletion	534-536	175-177	59	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	788-790	535-537	179	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	842-844	535-537	179	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	785-787	535-537	179	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634761	17:7674876-7674879	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	795-797	535-537	179	V/-	GTG/-	rs1597367938	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	795	653	218	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	653	653	218	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	653	653	218	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	786	653	218	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	789	653	218	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	786	653	218	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=351;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	535	257	86	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	535	257	86	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	909	-	-	-	-	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=238;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	389	257	86	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	535	257	86	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	453	374	125	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1291;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=284;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	903	536	179	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	786	536	179	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	535	176	59	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	535	176	59	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	535	176	59	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	789	536	179	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	843	536	179	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	786	536	179	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1754112	17:7674878-7674878	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	796	536	179	V/E	gTg/gAg	COSV52690974,COSV52712839,COSV52761003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	793-794	651-652	217-218	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	651-652	651-652	217-218	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	651-652	651-652	217-218	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	784-785	651-652	217-218	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	787-788	651-652	217-218	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	784-785	651-652	217-218	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=349;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	533-534	255-256	85-86	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	533-534	255-256	85-86	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	907-908	-	-	-	-	rs1567551279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=236;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	387-388	255-256	85-86	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	533-534	255-256	85-86	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	451-452	372-373	124-125	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567551279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567551279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1292;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=282;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	901-902	534-535	178-179	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	784-785	534-535	178-179	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	533-534	174-175	58-59	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	533-534	174-175	58-59	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	533-534	174-175	58-59	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	787-788	534-535	178-179	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	841-842	534-535	178-179	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	784-785	534-535	178-179	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634681	17:7674879-7674879	CACCA	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	794-795	534-535	178-179	-/WX	-/TGGTG	rs1567551279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	791	649	217	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	649	649	217	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	649	649	217	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	782	649	217	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	785	649	217	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	782	649	217	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM035961,COSV53163407,COSV53713958	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=347;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	531	253	85	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	531	253	85	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	905	-	-	-	-	CM035961,COSV53163407,COSV53713958	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM035961,COSV53163407,COSV53713958	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=234;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	385	253	85	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	531	253	85	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	449	370	124	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	CM035961,COSV53163407,COSV53713958	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM035961,COSV53163407,COSV53713958	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1295;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM035961,COSV53163407,COSV53713958	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=280;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	899	532	178	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	782	532	178	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	531	172	58	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	531	172	58	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	531	172	58	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	785	532	178	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	839	532	178	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	782	532	178	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1753870	17:7674881-7674882	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	792	532	178	V/X	Gtg/tg	CM035961,COSV53163407,COSV53713958	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	787	645	215	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	645	645	215	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	645	645	215	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	778	645	215	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	781	645	215	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	778	645	215	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=343;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	527	249	83	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	527	249	83	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	901	-	-	-	-	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=230;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	381	249	83	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	527	249	83	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	445	366	122	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1299;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=276;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	895	528	176	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	778	528	176	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	527	168	56	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	527	168	56	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	527	168	56	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	781	528	176	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	835	528	176	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	778	528	176	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1454254	17:7674885-7674886	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	788	528	176	S/X	agT/ag	CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	786-787	644-645	215	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	644-645	644-645	215	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	644-645	644-645	215	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	777-778	644-645	215	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	780-781	644-645	215	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	777-778	644-645	215	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=342;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	526-527	248-249	83	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	526-527	248-249	83	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	900-901	-	-	-	-	rs1555525759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=229;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	380-381	248-249	83	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	526-527	248-249	83	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	444-445	365-366	122	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1299;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=275;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	894-895	527-528	176	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	777-778	527-528	176	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	526-527	167-168	56	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	526-527	167-168	56	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	526-527	167-168	56	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	780-781	527-528	176	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	834-835	527-528	176	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	777-778	527-528	176	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492747	17:7674886-7674886	CT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	787-788	527-528	176	S/RX	agt/agAGt	rs1555525759	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	786	644	215	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	644	644	215	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	644	644	215	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	777	644	215	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	780	644	215	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	777	644	215	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=342;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	526	248	83	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	526	248	83	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	900	-	-	-	-	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=229;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	380	248	83	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	526	248	83	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	444	365	122	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1300;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=275;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	894	527	176	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	777	527	176	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	526	167	56	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	526	167	56	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	526	167	56	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	780	527	176	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	834	527	176	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	777	527	176	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
864318	17:7674886-7674887	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	787	527	176	S/X	aGt/at	COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	786	644	215	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	644	644	215	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	644	644	215	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	777	644	215	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	780	644	215	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	777	644	215	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=342;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	526	248	83	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	526	248	83	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	900	-	-	-	-	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=229;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	380	248	83	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	526	248	83	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	444	365	122	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1300;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=275;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	894	527	176	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	777	527	176	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	526	167	56	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	526	167	56	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	526	167	56	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	780	527	176	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	834	527	176	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	777	527	176	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376660	17:7674887-7674887	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	787	527	176	S/I	aGt/aTt	rs587782177,COSV52679681,COSV52686793,COSV52700292,COSV52891297	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	785-786	643-644	215	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	643-644	643-644	215	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	643-644	643-644	215	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	776-777	643-644	215	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	779-780	643-644	215	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	776-777	643-644	215	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551402	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=341;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	525-526	247-248	83	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	525-526	247-248	83	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	899-900	-	-	-	-	rs1567551402	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551402	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=228;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	379-380	247-248	83	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	525-526	247-248	83	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	443-444	364-365	122	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567551402	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567551402	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1300;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551402	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=274;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	893-894	526-527	176	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	776-777	526-527	176	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	525-526	166-167	56	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	525-526	166-167	56	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	525-526	166-167	56	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	779-780	526-527	176	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	833-834	526-527	176	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	776-777	526-527	176	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634694	17:7674887-7674887	T	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	786-787	526-527	176	S/KX	agt/aAgt	rs1567551402	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	784-785	642-643	214-215	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	642-643	642-643	214-215	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	642-643	642-643	214-215	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	775-776	642-643	214-215	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	778-779	642-643	214-215	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	775-776	642-643	214-215	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368095	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=340;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	524-525	246-247	82-83	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	524-525	246-247	82-83	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	898-899	-	-	-	-	rs1597368095	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368095	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=227;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	378-379	246-247	82-83	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	524-525	246-247	82-83	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	442-443	363-364	121-122	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597368095	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597368095	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1301;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368095	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=273;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	892-893	525-526	175-176	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	775-776	525-526	175-176	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	524-525	165-166	55-56	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	524-525	165-166	55-56	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	524-525	165-166	55-56	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	778-779	525-526	175-176	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	832-833	525-526	175-176	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	775-776	525-526	175-176	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
826394	17:7674887-7674889	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	785-786	525-526	175-176	HS/QX	caTAgt/cagt	rs1597368095	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	782	640	214	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	640	640	214	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	640	640	214	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	773	640	214	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	776	640	214	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	773	640	214	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52795913,COSV52851768,COSV52978286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=338;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	522	244	82	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	522	244	82	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	896	-	-	-	-	COSV52795913,COSV52851768,COSV52978286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52795913,COSV52851768,COSV52978286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=225;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	376	244	82	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	522	244	82	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	440	361	121	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52795913,COSV52851768,COSV52978286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52795913,COSV52851768,COSV52978286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1304;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52795913,COSV52851768,COSV52978286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=271;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	890	523	175	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	773	523	175	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	522	163	55	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	522	163	55	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	522	163	55	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	776	523	175	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	830	523	175	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	773	523	175	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1802476	17:7674890-7674891	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	783	523	175	H/X	Cat/at	COSV52795913,COSV52851768,COSV52978286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	783	641	214	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	641	641	214	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	641	641	214	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	774	641	214	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	777	641	214	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	774	641	214	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=339;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	523	245	82	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	523	245	82	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	897	-	-	-	-	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=226;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	377	245	82	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	523	245	82	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	441	362	121	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1303;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=272;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	891	524	175	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	774	524	175	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	523	164	55	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	523	164	55	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	523	164	55	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	777	524	175	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	831	524	175	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	774	524	175	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376615	17:7674890-7674890	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	784	524	175	H/R	cAt/cGt	rs1057519992,CM103210,COSV52670202,COSV52732998,COSV52834506,COSV52887765	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	770-781	628-639	210-213	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	628-639	628-639	210-213	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	628-639	628-639	210-213	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	761-772	628-639	210-213	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	764-775	628-639	210-213	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	761-772	628-639	210-213	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=326;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	510-521	232-243	78-81	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	510-521	232-243	78-81	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	884-895	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=213;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	364-375	232-243	78-81	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	510-521	232-243	78-81	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000514944.5	Transcript	inframe_deletion	428-439	349-360	117-120	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1305;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=259;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	878-889	511-522	171-174	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	761-772	511-522	171-174	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000610623.4	Transcript	inframe_deletion	510-521	151-162	51-54	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000618944.4	Transcript	inframe_deletion	510-521	151-162	51-54	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000619186.4	Transcript	inframe_deletion	510-521	151-162	51-54	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	764-775	511-522	171-174	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	818-829	511-522	171-174	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	761-772	511-522	171-174	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984966	17:7674891-7674903	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	771-782	511-522	171-174	NTFR/-	AACACTTTTCGA/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	778	636	212	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	636	636	212	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	636	636	212	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	769	636	212	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	772	636	212	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	769	636	212	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs864309495,CD011205,COSV52729299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=334;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	518	240	80	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	518	240	80	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	892	-	-	-	-	rs864309495,CD011205,COSV52729299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864309495,CD011205,COSV52729299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=221;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	372	240	80	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	518	240	80	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	436	357	119	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs864309495,CD011205,COSV52729299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs864309495,CD011205,COSV52729299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1308;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864309495,CD011205,COSV52729299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=267;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	886	519	173	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	769	519	173	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	518	159	53	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	518	159	53	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	518	159	53	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	772	519	173	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	826	519	173	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	769	519	173	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
218342	17:7674894-7674895	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	779	519	173	F/X	ttT/tt	rs864309495,CD011205,COSV52729299	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	779	637	213	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	637	637	213	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	637	637	213	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	770	637	213	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	773	637	213	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	770	637	213	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=335;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	519	241	81	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	519	241	81	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	893	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=222;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	373	241	81	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	519	241	81	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	437	358	120	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1307;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=268;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	887	520	174	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	770	520	174	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	519	160	54	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	519	160	54	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	519	160	54	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	773	520	174	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	827	520	174	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	770	520	174	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376651	17:7674894-7674894	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	780	520	174	R/G	Cga/Gga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	777-778	635-636	212	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	635-636	635-636	212	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	635-636	635-636	212	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	768-769	635-636	212	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	771-772	635-636	212	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	768-769	635-636	212	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs864309495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=333;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	517-518	239-240	80	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	517-518	239-240	80	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	891-892	-	-	-	-	rs864309495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864309495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=220;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	371-372	239-240	80	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	517-518	239-240	80	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	435-436	356-357	119	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs864309495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs864309495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1308;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864309495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=266;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	885-886	518-519	173	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	768-769	518-519	173	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	517-518	158-159	53	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	517-518	158-159	53	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	517-518	158-159	53	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	771-772	518-519	173	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	825-826	518-519	173	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	768-769	518-519	173	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428894	17:7674894-7674896	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	778-779	518-519	173	F/X	tTT/t	rs864309495	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	779	637	213	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	637	637	213	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	637	637	213	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	770	637	213	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	773	637	213	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	770	637	213	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=335;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	519	241	81	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	519	241	81	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	893	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=222;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	373	241	81	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	519	241	81	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	437	358	120	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1307;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=268;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	887	520	174	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	770	520	174	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	519	160	54	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	519	160	54	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	519	160	54	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	773	520	174	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	827	520	174	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	770	520	174	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
43590	17:7674894-7674894	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	780	520	174	R/*	Cga/Tga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	773-774	631-632	211	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	631-632	631-632	211	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	631-632	631-632	211	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	764-765	631-632	211	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	767-768	631-632	211	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	764-765	631-632	211	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=329;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	513-514	235-236	79	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	513-514	235-236	79	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	887-888	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=216;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	367-368	235-236	79	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	513-514	235-236	79	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	431-432	352-353	118	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1312;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=262;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	881-882	514-515	172	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	764-765	514-515	172	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	513-514	154-155	52	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	513-514	154-155	52	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	513-514	154-155	52	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	767-768	514-515	172	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	821-822	514-515	172	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	764-765	514-515	172	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1752799	17:7674898-7674900	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	774-775	514-515	172	T/X	ACt/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	770-771	628-629	210	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	628-629	628-629	210	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	628-629	628-629	210	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	761-762	628-629	210	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	764-765	628-629	210	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	761-762	628-629	210	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587776768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=326;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	510-511	232-233	78	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	510-511	232-233	78	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	884-885	-	-	-	-	rs587776768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587776768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=213;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	364-365	232-233	78	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	510-511	232-233	78	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	428-429	349-350	117	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs587776768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587776768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1315;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587776768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=259;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	878-879	511-512	171	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	761-762	511-512	171	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	510-511	151-152	51	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	510-511	151-152	51	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	510-511	151-152	51	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	764-765	511-512	171	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	818-819	511-512	171	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	761-762	511-512	171	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12361	17:7674901-7674903	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	771-772	511-512	171	N/X	AAc/c	rs587776768	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	768-769	626-627	209	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	626-627	626-627	209	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	626-627	626-627	209	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	759-760	626-627	209	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	762-763	626-627	209	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	759-760	626-627	209	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057517840	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=324;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	508-509	230-231	77	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	508-509	230-231	77	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	882-883	-	-	-	-	rs1057517840	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057517840	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=211;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	362-363	230-231	77	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	508-509	230-231	77	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	426-427	347-348	116	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1057517840	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057517840	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1317;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057517840	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=257;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	876-877	509-510	170	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	759-760	509-510	170	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	508-509	149-150	50	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	508-509	149-150	50	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	508-509	149-150	50	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	762-763	509-510	170	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	816-817	509-510	170	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	759-760	509-510	170	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
372539	17:7674903-7674905	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	769-770	509-510	170	R/X	aGA/a	rs1057517840	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	768-769	626-627	209	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	626-627	626-627	209	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	626-627	626-627	209	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	759-760	626-627	209	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	762-763	626-627	209	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	759-760	626-627	209	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52888898	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=324;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	508-509	230-231	77	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	508-509	230-231	77	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	882-883	-	-	-	-	COSV52888898	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52888898	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=211;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	362-363	230-231	77	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	508-509	230-231	77	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	426-427	347-348	116	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52888898	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52888898	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1317;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52888898	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=257;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	876-877	509-510	170	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	759-760	509-510	170	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	508-509	149-150	50	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	508-509	149-150	50	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	508-509	149-150	50	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	762-763	509-510	170	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	816-817	509-510	170	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	759-760	509-510	170	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
952244	17:7674904-7674904	C	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	769-770	509-510	170	R/RX	aga/agGa	COSV52888898	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	757	615	205	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	615	615	205	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	615	615	205	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	748	615	205	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	751	615	205	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	748	615	205	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=313;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	497	219	73	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	497	219	73	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	871	-	-	-	-	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=200;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	351	219	73	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	497	219	73	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	415	336	112	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1329;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=246;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	865	498	166	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	748	498	166	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	497	138	46	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	497	138	46	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	497	138	46	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	751	498	166	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	805	498	166	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	748	498	166	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185498	17:7674916-7674916	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	758	498	166	Y/*	taT/taA	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	757	615	205	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	615	615	205	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	615	615	205	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	748	615	205	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	751	615	205	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	748	615	205	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=313;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	497	219	73	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	497	219	73	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	871	-	-	-	-	COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=200;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	351	219	73	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	497	219	73	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	415	336	112	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1329;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=246;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	865	498	166	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	748	498	166	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	497	138	46	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	497	138	46	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	497	138	46	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	751	498	166	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	805	498	166	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	748	498	166	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839056	17:7674916-7674916	C	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	758	498	166	Y/*	taT/taG	COSV52713698,COSV52808763,COSV52840738	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	756	614	205	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	614	614	205	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	614	614	205	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	747	614	205	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	750	614	205	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	747	614	205	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=312;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	496	218	73	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	496	218	73	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	870	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=199;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	350	218	73	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	496	218	73	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	414	335	112	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1330;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=245;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	864	497	166	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	747	497	166	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	496	137	46	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	496	137	46	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	496	137	46	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	750	497	166	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	804	497	166	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	747	497	166	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376681	17:7674917-7674917	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	757	497	166	Y/C	tAt/tGt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	756	614	205	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	614	614	205	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	614	614	205	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	747	614	205	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	750	614	205	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	747	614	205	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=312;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	496	218	73	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	496	218	73	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	870	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=199;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	350	218	73	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	496	218	73	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	414	335	112	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1330;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=245;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	864	497	166	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	747	497	166	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	496	137	46	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	496	137	46	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	496	137	46	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	750	497	166	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	804	497	166	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	747	497	166	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376682	17:7674917-7674917	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	757	497	166	Y/F	tAt/tTt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	756	614	205	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	614	614	205	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	614	614	205	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	747	614	205	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	750	614	205	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	747	614	205	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=312;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	496	218	73	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	496	218	73	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	870	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=199;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	350	218	73	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	496	218	73	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	414	335	112	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1330;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=245;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	864	497	166	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	747	497	166	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	496	137	46	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	496	137	46	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	496	137	46	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	750	497	166	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	804	497	166	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	747	497	166	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376683	17:7674917-7674917	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	757	497	166	Y/S	tAt/tCt	rs1057520007,COSV52665440,COSV52677268,COSV52688506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	736-753	594-611	198-204	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	594-611	594-611	198-204	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	594-611	594-611	198-204	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	727-744	594-611	198-204	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	730-747	594-611	198-204	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	727-744	594-611	198-204	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=292;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	476-493	198-215	66-72	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	476-493	198-215	66-72	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	850-867	-	-	-	-	rs1567551704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=179;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	330-347	198-215	66-72	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	476-493	198-215	66-72	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000514944.5	Transcript	inframe_deletion	394-411	315-332	105-111	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567551704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567551704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1333;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=225;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	844-861	477-494	159-165	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	727-744	477-494	159-165	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000610623.4	Transcript	inframe_deletion	476-493	117-134	39-45	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000618944.4	Transcript	inframe_deletion	476-493	117-134	39-45	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000619186.4	Transcript	inframe_deletion	476-493	117-134	39-45	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	730-747	477-494	159-165	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	784-801	477-494	159-165	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	727-744	477-494	159-165	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
560921	17:7674919-7674937	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	737-754	477-494	159-165	EGNLRVE/E	gaAGGAAATTTGCGTGTGGAg/gag	rs1567551704	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	751-752	609-610	203-204	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	609-610	609-610	203-204	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	609-610	609-610	203-204	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	742-743	609-610	203-204	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	745-746	609-610	203-204	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	742-743	609-610	203-204	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551718,COSV53117470	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=307;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	491-492	213-214	71-72	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	491-492	213-214	71-72	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	865-866	-	-	-	-	rs1567551718,COSV53117470	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551718,COSV53117470	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=194;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	345-346	213-214	71-72	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	491-492	213-214	71-72	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	409-410	330-331	110-111	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567551718,COSV53117470	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567551718,COSV53117470	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1334;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551718,COSV53117470	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=240;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	859-860	492-493	164-165	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	742-743	492-493	164-165	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	491-492	132-133	44-45	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	491-492	132-133	44-45	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	491-492	132-133	44-45	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	745-746	492-493	164-165	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	799-800	492-493	164-165	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	742-743	492-493	164-165	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634764	17:7674921-7674922	AG	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	752-753	492-493	164-165	VE/V*	gtGGag/gtCTag	rs1567551718,COSV53117470	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	752	610	204	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	610	610	204	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	610	610	204	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	743	610	204	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	746	610	204	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	743	610	204	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=308;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	492	214	72	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	492	214	72	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	866	-	-	-	-	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=195;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	346	214	72	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	492	214	72	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	410	331	111	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1334;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=241;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	860	493	165	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	743	493	165	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	492	133	45	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	492	133	45	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	492	133	45	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	746	493	165	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	800	493	165	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	743	493	165	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
977783	17:7674921-7674921	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	753	493	165	E/*	Gag/Tag	rs2073336758,COSV52679869,COSV53267121,COSV53424574	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	744-745	602-603	201	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	602-603	602-603	201	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	602-603	602-603	201	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	735-736	602-603	201	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	738-739	602-603	201	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	735-736	602-603	201	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104584740,COSV53023337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=300;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	484-485	206-207	69	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	484-485	206-207	69	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	858-859	-	-	-	-	COSV104584740,COSV53023337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104584740,COSV53023337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=187;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	338-339	206-207	69	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	484-485	206-207	69	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	402-403	323-324	108	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV104584740,COSV53023337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104584740,COSV53023337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1341;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104584740,COSV53023337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=233;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	852-853	485-486	162	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	735-736	485-486	162	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	484-485	125-126	42	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	484-485	125-126	42	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	484-485	125-126	42	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	738-739	485-486	162	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	792-793	485-486	162	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	735-736	485-486	162	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1751170	17:7674928-7674928	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	745-746	485-486	162	L/FX	ttg/ttTg	COSV104584740,COSV53023337	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	744	602	201	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	602	602	201	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	602	602	201	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	735	602	201	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	738	602	201	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	735	602	201	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52837759,COSV53037685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=300;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	484	206	69	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	484	206	69	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	858	-	-	-	-	COSV52837759,COSV53037685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52837759,COSV53037685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=187;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	338	206	69	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	484	206	69	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	402	323	108	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52837759,COSV53037685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52837759,COSV53037685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1342;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52837759,COSV53037685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=233;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	852	485	162	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	735	485	162	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	484	125	42	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	484	125	42	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	484	125	42	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	738	485	162	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	792	485	162	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	735	485	162	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
924862	17:7674928-7674929	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	745	485	162	L/X	tTg/tg	COSV52837759,COSV53037685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	741	599	200	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	599	599	200	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	599	599	200	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	732	599	200	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	735	599	200	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	732	599	200	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=297;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	481	203	68	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	481	203	68	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	855	-	-	-	-	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=184;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	335	203	68	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	481	203	68	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	399	320	107	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1345;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=230;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	849	482	161	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	732	482	161	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	481	122	41	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	481	122	41	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	481	122	41	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	735	482	161	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	789	482	161	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	732	482	161	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428870	17:7674931-7674932	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	742	482	161	N/X	aAt/at	rs1131691011,COSV52677283,COSV52840642,COSV53742336	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	738	596	199	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	596	596	199	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	596	596	199	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	729	596	199	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	732	596	199	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	729	596	199	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=294;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	478	200	67	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	478	200	67	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	852	-	-	-	-	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=181;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	332	200	67	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	478	200	67	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	396	317	106	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1348;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=227;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	846	479	160	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	729	479	160	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	478	119	40	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	478	119	40	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	478	119	40	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	732	479	160	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	786	479	160	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	729	479	160	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
451799	17:7674935-7674935	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	739	479	160	G/V	gGa/gTa	rs1555525857,COSV52661319,COSV52679535,COSV53326529	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	737	595	199	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	595	595	199	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	595	595	199	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	728	595	199	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	731	595	199	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	728	595	199	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=293;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	477	199	67	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	477	199	67	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	851	-	-	-	-	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=180;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	331	199	67	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	477	199	67	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	395	316	106	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1349;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=226;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	845	478	160	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	728	478	160	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	477	118	40	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	477	118	40	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	477	118	40	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	731	478	160	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	785	478	160	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	728	478	160	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634672	17:7674936-7674936	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	738	478	160	G/*	Gga/Tga	rs1567551821,COSV52710769,COSV52715098,COSV52760685	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	734	592	198	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	592	592	198	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	592	592	198	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	725	592	198	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	728	592	198	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	725	592	198	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=290;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	474	196	66	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	474	196	66	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	848	-	-	-	-	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=177;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	328	196	66	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	474	196	66	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	392	313	105	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1352;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=223;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	842	475	159	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	725	475	159	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	474	115	39	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	474	115	39	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	474	115	39	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	728	475	159	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	782	475	159	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	725	475	159	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428900	17:7674938-7674939	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	735	475	159	E/X	Gaa/aa	rs1131691035,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	734	592	198	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	592	592	198	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	592	592	198	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	725	592	198	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	728	592	198	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	725	592	198	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=290;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	474	196	66	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	474	196	66	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	848	-	-	-	-	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=177;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	328	196	66	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	474	196	66	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	392	313	105	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1352;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=223;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	842	475	159	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	725	475	159	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	474	115	39	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	474	115	39	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	474	115	39	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	728	475	159	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	782	475	159	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	725	475	159	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634704	17:7674939-7674939	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	735	475	159	E/*	Gaa/Taa	rs1567551854,COSV52678088,COSV52771688,COSV53175941	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	723-727	581-585	194-195	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	581-585	581-585	194-195	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	581-585	581-585	194-195	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	714-718	581-585	194-195	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	717-721	581-585	194-195	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	714-718	581-585	194-195	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=279;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	463-467	185-189	62-63	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	463-467	185-189	62-63	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	837-841	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=166;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	317-321	185-189	62-63	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	463-467	185-189	62-63	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	381-385	302-306	101-102	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1359;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=212;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	831-835	464-468	155-156	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	714-718	464-468	155-156	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	463-467	104-108	35-36	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	463-467	104-108	35-36	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	463-467	104-108	35-36	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	717-721	464-468	155-156	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	771-775	464-468	155-156	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	714-718	464-468	155-156	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1076187	17:7674945-7674950	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	724-728	464-468	155-156	LI/X	cTTATC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	728	586	196	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	586	586	196	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	586	586	196	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	719	586	196	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	722	586	196	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	719	586	196	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=284;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	468	190	64	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	468	190	64	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	842	-	-	-	-	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=171;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	322	190	64	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	468	190	64	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	386	307	103	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1358;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=217;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	836	469	157	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	719	469	157	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	468	109	37	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	468	109	37	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	468	109	37	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	722	469	157	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	776	469	157	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	719	469	157	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43589	17:7674945-7674945	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	729	469	157	R/*	Cga/Tga	rs397516435,CM941329,COSV52663748,COSV53125285,COSV53128268	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	724	582	194	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	582	582	194	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	582	582	194	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	715	582	194	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	718	582	194	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	715	582	194	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=280;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	464	186	62	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	464	186	62	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	838	-	-	-	-	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=167;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	318	186	62	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	464	186	62	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	382	303	101	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1362;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=213;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	832	465	155	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	715	465	155	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	464	105	35	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	464	105	35	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	464	105	35	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	718	465	155	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	772	465	155	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	715	465	155	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634675	17:7674948-7674949	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	725	465	155	L/X	ctT/ct	rs1567552031,COSV52772013,COSV52864400,COSV53143214	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	720-722	578-580	193-194	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	578-580	578-580	193-194	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	578-580	578-580	193-194	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	711-713	578-580	193-194	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	714-716	578-580	193-194	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	711-713	578-580	193-194	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=276;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	460-462	182-184	61-62	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	460-462	182-184	61-62	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	834-836	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=163;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	314-316	182-184	61-62	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	460-462	182-184	61-62	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	378-380	299-301	100-101	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1364;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=209;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	828-830	461-463	154-155	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	711-713	461-463	154-155	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	460-462	101-103	34-35	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	460-462	101-103	34-35	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	460-462	101-103	34-35	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	714-716	461-463	154-155	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	768-770	461-463	154-155	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	711-713	461-463	154-155	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1191520	17:7674951-7674953	TTTAGGTCTG	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	721-723	461-463	154-155	HL/PDLNX	cATCtt/cCAGACCTAAAtt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	721	579	193	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	579	579	193	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	579	579	193	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	712	579	193	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	715	579	193	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	712	579	193	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=277;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	461	183	61	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	461	183	61	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	835	-	-	-	-	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=164;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	315	183	61	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	461	183	61	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	379	300	100	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1365;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=210;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	829	462	154	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	712	462	154	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	461	102	34	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	461	102	34	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	461	102	34	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	715	462	154	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	769	462	154	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	712	462	154	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825975	17:7674952-7674952	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	722	462	154	H/Q	caT/caA	rs1597368777,COSV52924326,COSV53086641,COSV53219838	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	720	578	193	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	578	578	193	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	578	578	193	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	711	578	193	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	714	578	193	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	711	578	193	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=276;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	460	182	61	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	460	182	61	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	834	-	-	-	-	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=163;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	314	182	61	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	460	182	61	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	378	299	100	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1366;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=209;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	828	461	154	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	711	461	154	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	460	101	34	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	460	101	34	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	460	101	34	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	714	461	154	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	768	461	154	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	711	461	154	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376612	17:7674953-7674953	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	721	461	154	H/P	cAt/cCt	rs786201838,CM083194,CM951225,COSV106055109,COSV52662414,COSV52663304,COSV52681707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	719	577	193	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	577	577	193	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	577	577	193	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	710	577	193	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	713	577	193	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	710	577	193	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=275;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	459	181	61	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	459	181	61	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	833	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=162;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	313	181	61	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	459	181	61	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	377	298	100	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1367;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=208;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	827	460	154	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	710	460	154	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	459	100	34	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	459	100	34	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	459	100	34	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	713	460	154	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	767	460	154	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	710	460	154	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376613	17:7674954-7674954	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	720	460	154	H/D	Cat/Gat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	719	577	193	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	577	577	193	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	577	577	193	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	710	577	193	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	713	577	193	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	710	577	193	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=275;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	459	181	61	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	459	181	61	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	833	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=162;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	313	181	61	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	459	181	61	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	377	298	100	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1367;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=208;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	827	460	154	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	710	460	154	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	459	100	34	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	459	100	34	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	459	100	34	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	713	460	154	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	767	460	154	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	710	460	154	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376614	17:7674954-7674954	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	720	460	154	H/N	Cat/Aat	rs876658468,COSV52675896,COSV52688299,COSV52757395	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	717	575	192	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	575	575	192	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	575	575	192	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	708	575	192	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	711	575	192	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	708	575	192	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839714,COSV53416426	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=273;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	457	179	60	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	457	179	60	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	831	-	-	-	-	COSV52839714,COSV53416426	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839714,COSV53416426	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=160;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	311	179	60	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	457	179	60	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	375	296	99	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52839714,COSV53416426	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52839714,COSV53416426	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1369;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839714,COSV53416426	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=206;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	825	458	153	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	708	458	153	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	457	98	33	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	457	98	33	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	457	98	33	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	711	458	153	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	765	458	153	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	708	458	153	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1749472	17:7674955-7674956	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	718	458	153	Q/X	cAg/cg	COSV52839714,COSV53416426	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	714-716	572-574	191-192	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	572-574	572-574	191-192	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	572-574	572-574	191-192	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	705-707	572-574	191-192	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	708-710	572-574	191-192	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	705-707	572-574	191-192	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=270;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	454-456	176-178	59-60	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	454-456	176-178	59-60	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	828-830	-	-	-	-	rs1555525902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=157;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	308-310	176-178	59-60	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	454-456	176-178	59-60	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000514944.5	Transcript	inframe_deletion	372-374	293-295	98-99	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1370;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=203;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	822-824	455-457	152-153	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	705-707	455-457	152-153	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000610623.4	Transcript	inframe_deletion	454-456	95-97	32-33	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000618944.4	Transcript	inframe_deletion	454-456	95-97	32-33	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000619186.4	Transcript	inframe_deletion	454-456	95-97	32-33	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	708-710	455-457	152-153	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	762-764	455-457	152-153	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	705-707	455-457	152-153	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
458551	17:7674956-7674959	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	715-717	455-457	152-153	PQ/Q	cCTCag/cag	rs1555525902	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	716	574	192	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	574	574	192	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	574	574	192	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	707	574	192	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	710	574	192	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	707	574	192	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs866380588,COSV52660737,COSV52978302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=272;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	456	178	60	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	456	178	60	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	830	-	-	-	-	rs866380588,COSV52660737,COSV52978302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs866380588,COSV52660737,COSV52978302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=159;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	310	178	60	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	456	178	60	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	374	295	99	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs866380588,COSV52660737,COSV52978302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs866380588,COSV52660737,COSV52978302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1370;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs866380588,COSV52660737,COSV52978302	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=205;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	824	457	153	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	707	457	153	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	456	97	33	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	456	97	33	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	456	97	33	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	710	457	153	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	764	457	153	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	707	457	153	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
406579	17:7674957-7674957	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	717	457	153	Q/*	Cag/Tag	rs866380588,COSV52660737,COSV52978302	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	715	573	191	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	573	573	191	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	573	573	191	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	706	573	191	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	709	573	191	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	706	573	191	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53772983,COSV99359984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=271;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	455	177	59	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	455	177	59	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	829	-	-	-	-	COSV53772983,COSV99359984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53772983,COSV99359984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=158;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	309	177	59	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	455	177	59	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	373	294	98	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV53772983,COSV99359984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53772983,COSV99359984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1371;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53772983,COSV99359984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=204;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	823	456	152	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	706	456	152	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	455	96	32	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	455	96	32	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	455	96	32	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	709	456	152	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	763	456	152	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	706	456	152	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
964947	17:7674957-7674958	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	716	456	152	P/X	ccT/cc	COSV53772983,COSV99359984	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	713-714	571-572	191	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	571-572	571-572	191	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	571-572	571-572	191	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	704-705	571-572	191	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	707-708	571-572	191	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	704-705	571-572	191	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=269;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	453-454	175-176	59	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	453-454	175-176	59	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	827-828	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=156;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	307-308	175-176	59	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	453-454	175-176	59	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	371-372	292-293	98	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1372;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=202;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	821-822	454-455	152	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	704-705	454-455	152	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	453-454	94-95	32	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	453-454	94-95	32	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	453-454	94-95	32	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	707-708	454-455	152	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	761-762	454-455	152	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	704-705	454-455	152	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1438732	17:7674959-7674959	ACCT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	714-715	454-455	152	P/QVX	cct/cAGGTct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	711	569	190	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	569	569	190	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	569	569	190	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	702	569	190	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	705	569	190	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	702	569	190	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=267;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	451	173	58	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	451	173	58	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	825	-	-	-	-	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=154;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	305	173	58	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	451	173	58	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	369	290	97	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1375;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=200;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	819	452	151	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	702	452	151	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	451	92	31	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	451	92	31	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	451	92	31	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	705	452	151	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	759	452	151	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	702	452	151	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
825904	17:7674961-7674962	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	712	452	151	P/X	cCt/ct	rs1597368891,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	711	569	190	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	569	569	190	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	569	569	190	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	702	569	190	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	705	569	190	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	702	569	190	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=267;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	451	173	58	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	451	173	58	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	825	-	-	-	-	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=154;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	305	173	58	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	451	173	58	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	369	290	97	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1375;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=200;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	819	452	151	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	702	452	151	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	451	92	31	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	451	92	31	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	451	92	31	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	705	452	151	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	759	452	151	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	702	452	151	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
418517	17:7674962-7674962	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	712	452	151	P/L	cCt/cTt	rs876660825,CM161004,COSV52664064,COSV52987047,COSV53313892	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	707-708	565-566	189	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	565-566	565-566	189	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	565-566	565-566	189	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	698-699	565-566	189	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	701-702	565-566	189	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	698-699	565-566	189	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52827240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=263;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	447-448	169-170	57	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	447-448	169-170	57	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	821-822	-	-	-	-	COSV52827240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52827240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=150;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	301-302	169-170	57	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	447-448	169-170	57	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	365-366	286-287	96	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52827240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52827240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1378;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52827240	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=196;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	815-816	448-449	150	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	698-699	448-449	150	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	447-448	88-89	30	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	447-448	88-89	30	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	447-448	88-89	30	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	701-702	448-449	150	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	755-756	448-449	150	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	698-699	448-449	150	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
953178	17:7674964-7674966	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	708-709	448-449	150	A/X	GCc/c	COSV52827240	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-708	?-566	?-189	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5-6/11;INTRON=4-5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-566	?-566	?-189	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4-5/9;INTRON=3-4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-566	?-566	?-189	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4-5/7;INTRON=3-4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-699	?-566	?-189	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5-6/12;INTRON=4-5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-702	?-566	?-189	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5-6/11;INTRON=4-5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-699	?-566	?-189	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5-6/12;INTRON=4-5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,5_prime_UTR_variant,intron_variant	62-448	?-170	?-57	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-2/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,5_prime_UTR_variant,intron_variant	62-448	?-170	?-57	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-2/7;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,non_coding_transcript_exon_variant,intron_variant	?-822	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4-5/5;INTRON=3-4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant	?-302	?-170	?-57	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2-3/6;INTRON=1-2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,5_prime_UTR_variant,intron_variant	62-448	?-170	?-57	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-2/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-366	?-287	?-96	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4-5/6;INTRON=3-4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000574684.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,non_coding_transcript_exon_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1378;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-816	?-449	?-150	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4-5/10;INTRON=3-4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-699	?-449	?-150	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5-6/12;INTRON=4-5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,5_prime_UTR_variant,intron_variant	62-448	?-89	?-30	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-2/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,5_prime_UTR_variant,intron_variant	62-448	?-89	?-30	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-2/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,start_lost,splice_polypyrimidine_tract_variant,5_prime_UTR_variant,intron_variant	62-448	?-89	?-30	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1-2/7;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-702	?-449	?-150	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5-6/11;INTRON=4-5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-756	?-449	?-150	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5-6/11;INTRON=4-5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-699	?-449	?-150	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5-6/12;INTRON=4-5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
961330	17:7674964-7675432	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,splice_donor_variant,splice_donor_5th_base_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant,NMD_transcript_variant	?-709	?-449	?-150	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5-6/12;INTRON=4-5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	706-707	564-565	188-189	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	564-565	564-565	188-189	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	564-565	564-565	188-189	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	697-698	564-565	188-189	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	700-701	564-565	188-189	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	697-698	564-565	188-189	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99036713	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=262;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	446-447	168-169	56-57	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	446-447	168-169	56-57	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	820-821	-	-	-	-	COSV99036713	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99036713	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=149;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	300-301	168-169	56-57	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	446-447	168-169	56-57	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	364-365	285-286	95-96	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV99036713	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99036713	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1379;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99036713	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=195;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	814-815	447-448	149-150	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	697-698	447-448	149-150	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	446-447	87-88	29-30	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	446-447	87-88	29-30	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	446-447	87-88	29-30	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	700-701	447-448	149-150	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	754-755	447-448	149-150	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	697-698	447-448	149-150	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
848780	17:7674966-7674966	CAGA	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	707-708	447-448	149-150	-/SX	-/TCTG	COSV99036713	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	705	563	188	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	563	563	188	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	563	563	188	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	696	563	188	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	699	563	188	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	696	563	188	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=261;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	445	167	56	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	445	167	56	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	819	-	-	-	-	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=148;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	299	167	56	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	445	167	56	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	363	284	95	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1381;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=194;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	813	446	149	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	696	446	149	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	445	86	29	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	445	86	29	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	445	86	29	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	699	446	149	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	753	446	149	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	696	446	149	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
825864	17:7674967-7674968	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	706	446	149	L/X	cTg/cg	rs1597368970,CM101594,COSV53828607,COSV53839074	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501212	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=254;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501212	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=141;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1060501212	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501212	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1386;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501212	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=187;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406611	17:7674972-7674975	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1060501212	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=257;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=144;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1385;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=190;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
492748	17:7674972-7674972	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=257;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=144;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1385;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=190;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634769	17:7674972-7674972	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs1202793339,CD043957,CS011574,CS083991,COSV52662318,COSV52676510,COSV52683087,COSV52690533	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=256;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=143;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1386;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=189;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1189743	17:7674973-7674973	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	CS150685,CS941545,COSV52664494,COSV52666095,COSV52685228	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=255;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=142;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1387;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=188;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634683	17:7674974-7674974	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs763746485,COSV52679067	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=239;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=126;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1393;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=172;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
853317	17:7674979-7674990	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=178;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=65;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000574684.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1459;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=111;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1068426	17:7675045-7675051	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	664-?	522-?	174-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	522-?	522-?	174-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	522-?	522-?	174-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	655-?	522-?	174-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	658-?	522-?	174-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	655-?	522-?	174-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=139;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	404-?	126-?	42-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	404-?	126-?	42-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,non_coding_transcript_exon_variant,intron_variant	778-?	-	-	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=26;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	258-?	126-?	42-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	404-?	126-?	42-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	322-?	243-?	81-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000574684.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,non_coding_transcript_exon_variant,intron_variant	30-?	-	-	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1461;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=72;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	772-?	405-?	135-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	655-?	405-?	135-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	404-?	45-?	15-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	404-?	45-?	15-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	404-?	45-?	15-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	658-?	405-?	135-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	712-?	405-?	135-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	655-?	405-?	135-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528272	17:7675047-7675090	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant,NMD_transcript_variant	665-?	405-?	135-?	-	-	rs1555525957	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=178;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=65;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000574684.1	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1464;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=111;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
633019	17:7675050-7675051	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1567552459,CS114004,COSV52709511,COSV52900265,COSV53486980,COSV99478821	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369390	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=178;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369390	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=65;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000574684.1	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597369390	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1463;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369390	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=111;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
825842	17:7675050-7675051	AC	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,splice_donor_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1597369390	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,coding_sequence_variant	683-?	541-?	181-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,coding_sequence_variant	541-?	541-?	181-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant,coding_sequence_variant	541-?	541-?	181-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,coding_sequence_variant	674-?	541-?	181-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,coding_sequence_variant	677-?	541-?	181-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,coding_sequence_variant	674-?	541-?	181-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=158;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant,coding_sequence_variant	423-?	145-?	49-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant,coding_sequence_variant	423-?	145-?	49-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_exon_variant	797-?	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=45;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant,coding_sequence_variant	277-?	145-?	49-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant,coding_sequence_variant	423-?	145-?	49-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant,coding_sequence_variant	341-?	262-?	88-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000574684.1	Transcript	splice_donor_variant,non_coding_transcript_exon_variant	49-?	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1465;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=91;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,coding_sequence_variant	791-?	424-?	142-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,coding_sequence_variant	674-?	424-?	142-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant,coding_sequence_variant	423-?	64-?	22-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant,coding_sequence_variant	423-?	64-?	22-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant,coding_sequence_variant	423-?	64-?	22-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,coding_sequence_variant	677-?	424-?	142-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,coding_sequence_variant	731-?	424-?	142-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,coding_sequence_variant	674-?	424-?	142-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1747376	17:7675051-7675071	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,coding_sequence_variant,NMD_transcript_variant	684-?	424-?	142-?	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,coding_sequence_variant	699-?	557-?	186-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,coding_sequence_variant	557-?	557-?	186-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant,coding_sequence_variant	557-?	557-?	186-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,coding_sequence_variant	690-?	557-?	186-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,coding_sequence_variant	693-?	557-?	186-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,coding_sequence_variant	690-?	557-?	186-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552467,COSV53341088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=174;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant,coding_sequence_variant	439-?	161-?	54-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant,coding_sequence_variant	439-?	161-?	54-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_exon_variant	813-?	-	-	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552467,COSV53341088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=61;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant,coding_sequence_variant	293-?	161-?	54-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant,coding_sequence_variant	439-?	161-?	54-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant,coding_sequence_variant	357-?	278-?	93-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000574684.1	Transcript	splice_donor_variant,non_coding_transcript_exon_variant	65-?	-	-	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567552467,COSV53341088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1464;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552467,COSV53341088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=107;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,coding_sequence_variant	807-?	440-?	147-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,coding_sequence_variant	690-?	440-?	147-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant,coding_sequence_variant	439-?	80-?	27-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant,coding_sequence_variant	439-?	80-?	27-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant,coding_sequence_variant	439-?	80-?	27-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,coding_sequence_variant	693-?	440-?	147-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,coding_sequence_variant	747-?	440-?	147-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,coding_sequence_variant	690-?	440-?	147-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
633020	17:7675051-7675055	CCCC	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,coding_sequence_variant,NMD_transcript_variant	700-?	440-?	147-?	-	-	rs1567552467,COSV53341088	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=177;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=64;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000574684.1	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1465;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=110;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428908	17:7675052-7675052	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=177;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=64;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000574684.1	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1465;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=110;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
649747	17:7675052-7675052	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1131691042,CS137624,CS167574,COSV52670017,COSV52686439,COSV52695669	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	693-696	551-554	184-185	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	551-554	551-554	184-185	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	551-554	551-554	184-185	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	684-687	551-554	184-185	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	687-690	551-554	184-185	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	684-687	551-554	184-185	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=168;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	433-436	155-158	52-53	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	433-436	155-158	52-53	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	807-810	-	-	-	-	rs1597369519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=55;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	287-290	155-158	52-53	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	433-436	155-158	52-53	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	351-354	272-275	91-92	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	59-62	-	-	-	-	rs1597369519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597369519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1471;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=101;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	801-804	434-437	145-146	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	684-687	434-437	145-146	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	433-436	74-77	25-26	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	433-436	74-77	25-26	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	433-436	74-77	25-26	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	687-690	434-437	145-146	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	741-744	434-437	145-146	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	684-687	434-437	145-146	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
639824	17:7675057-7675061	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	694-697	434-437	145-146	DS/X	gATAGc/gc	rs1597369519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	693	551	184	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	551	551	184	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	551	551	184	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	684	551	184	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	687	551	184	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	684	551	184	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552536,COSV53082292	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=168;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	433	155	52	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	433	155	52	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	807	-	-	-	-	rs1567552536,COSV53082292	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552536,COSV53082292	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=55;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	287	155	52	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	433	155	52	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	351	272	91	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	59	-	-	-	-	rs1567552536,COSV53082292	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567552536,COSV53082292	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1474;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552536,COSV53082292	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=101;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	801	434	145	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	684	434	145	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	433	74	25	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	433	74	25	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	433	74	25	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	687	434	145	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	741	434	145	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	684	434	145	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634765	17:7675060-7675061	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	694	434	145	D/X	gAt/gt	rs1567552536,COSV53082292	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	690	548	183	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	548	548	183	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	548	548	183	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	681	548	183	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	684	548	183	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	681	548	183	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=165;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	430	152	51	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	430	152	51	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	804	-	-	-	-	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=52;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	284	152	51	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	430	152	51	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	348	269	90	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	56	-	-	-	-	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1477;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=98;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	798	431	144	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	681	431	144	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	430	71	24	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	430	71	24	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	430	71	24	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	684	431	144	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	738	431	144	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	681	431	144	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634701	17:7675064-7675064	C	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	691	431	144	S/*	tCa/tGa	rs1555525970,COSV52662121,COSV52858115,COSV53050787,COSV53082360	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	687	545	182	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	545	545	182	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	545	545	182	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	678	545	182	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	681	545	182	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	678	545	182	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552584,COSV52661754,COSV52701277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=162;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	427	149	50	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	427	149	50	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	801	-	-	-	-	rs1567552584,COSV52661754,COSV52701277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552584,COSV52661754,COSV52701277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=49;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	281	149	50	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	427	149	50	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	345	266	89	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	53	-	-	-	-	rs1567552584,COSV52661754,COSV52701277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567552584,COSV52661754,COSV52701277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1480;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552584,COSV52661754,COSV52701277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=95;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	795	428	143	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	678	428	143	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	427	68	23	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	427	68	23	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	427	68	23	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	681	428	143	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	735	428	143	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	678	428	143	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634775	17:7675066-7675067	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	688	428	143	C/X	tGc/tc	rs1567552584,COSV52661754,COSV52701277	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	684	542	181	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	542	542	181	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	542	542	181	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	675	542	181	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	678	542	181	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	675	542	181	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=159;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	424	146	49	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	424	146	49	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	798	-	-	-	-	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=46;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	278	146	49	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	424	146	49	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	342	263	88	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	50	-	-	-	-	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1483;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=92;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	792	425	142	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	675	425	142	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	424	65	22	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	424	65	22	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	424	65	22	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	678	425	142	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	732	425	142	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	675	425	142	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
825729	17:7675070-7675070	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	685	425	142	R/P	cGc/cCc	rs397514495,CM056067,CM920671,CM942120,COSV52675795,COSV52676870,COSV52730435,COSV53567603	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	675-682	533-540	178-180	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	533-540	533-540	178-180	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	533-540	533-540	178-180	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	666-673	533-540	178-180	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	669-676	533-540	178-180	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	666-673	533-540	178-180	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=150;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	415-422	137-144	46-48	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	415-422	137-144	46-48	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	789-796	-	-	-	-	rs1567552637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=37;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	269-276	137-144	46-48	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	415-422	137-144	46-48	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	333-340	254-261	85-87	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	41-48	-	-	-	-	rs1567552637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567552637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1485;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=83;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	783-790	416-423	139-141	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	666-673	416-423	139-141	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	415-422	56-63	19-21	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	415-422	56-63	19-21	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	415-422	56-63	19-21	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	669-676	416-423	139-141	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	723-730	416-423	139-141	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	666-673	416-423	139-141	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634677	17:7675071-7675079	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	676-683	416-423	139-141	HHE/X	cACCATGAG/c	rs1567552637	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	680	538	180	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	538	538	180	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	538	538	180	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	671	538	180	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	674	538	180	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	671	538	180	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=155;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	420	142	48	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	420	142	48	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	794	-	-	-	-	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=42;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	274	142	48	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	420	142	48	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	338	259	87	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	46	-	-	-	-	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1487;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=88;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	788	421	141	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	671	421	141	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	420	61	21	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	420	61	21	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	420	61	21	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	674	421	141	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	728	421	141	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	671	421	141	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634687	17:7675074-7675074	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	681	421	141	E/*	Gag/Tag	rs879253911,CM941328,COSV52694461,COSV52816009,COSV53014483,COSV53470757	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	679	537	179	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	537	537	179	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	537	537	179	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	670	537	179	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	673	537	179	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	670	537	179	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=154;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	419	141	47	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	419	141	47	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	793	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=41;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	273	141	47	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	419	141	47	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	337	258	86	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	45	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1488;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=87;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	787	420	140	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	670	420	140	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	419	60	20	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	419	60	20	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	419	60	20	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	673	420	140	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	727	420	140	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	670	420	140	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376607	17:7675075-7675075	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	680	420	140	H/Q	caT/caG	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	679	537	179	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	537	537	179	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	537	537	179	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	670	537	179	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	673	537	179	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	670	537	179	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=154;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	419	141	47	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	419	141	47	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	793	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=41;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	273	141	47	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	419	141	47	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	337	258	86	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	45	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1488;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=87;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	787	420	140	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	670	420	140	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	419	60	20	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	419	60	20	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	419	60	20	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	673	420	140	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	727	420	140	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	670	420	140	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406578	17:7675075-7675075	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	680	420	140	H/Q	caT/caA	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	677-678	535-536	179	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	535-536	535-536	179	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	535-536	535-536	179	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	668-669	535-536	179	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	671-672	535-536	179	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	668-669	535-536	179	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=152;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	417-418	139-140	47	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	417-418	139-140	47	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	791-792	-	-	-	-	rs1567552753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=39;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	271-272	139-140	47	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	417-418	139-140	47	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	335-336	256-257	86	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	43-44	-	-	-	-	rs1567552753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567552753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1489;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=85;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	785-786	418-419	140	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	668-669	418-419	140	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	417-418	58-59	20	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	417-418	58-59	20	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	417-418	58-59	20	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	671-672	418-419	140	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	725-726	418-419	140	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	668-669	418-419	140	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
580994	17:7675076-7675076	GGTGGGGGCAGCGCCTCAC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	678-679	418-419	140	H/REALPPPX	cat/cGTGAGGCGCTGCCCCCACCat	rs1567552753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	674	532	178	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	532	532	178	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	532	532	178	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	665	532	178	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	668	532	178	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	665	532	178	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=149;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	414	136	46	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	414	136	46	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	788	-	-	-	-	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=36;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	268	136	46	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	414	136	46	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	332	253	85	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	40	-	-	-	-	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1493;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=82;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	782	415	139	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	665	415	139	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	414	55	19	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	414	55	19	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	414	55	19	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	668	415	139	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	722	415	139	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	665	415	139	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
12377	17:7675079-7675080	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	675	415	139	H/X	Cac/ac	rs786202525,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	674	532	178	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	532	532	178	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	532	532	178	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	665	532	178	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	668	532	178	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	665	532	178	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=149;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	414	136	46	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	414	136	46	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	788	-	-	-	-	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=36;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	268	136	46	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	414	136	46	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	332	253	85	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	40	-	-	-	-	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1493;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=82;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	782	415	139	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	665	415	139	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	414	55	19	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	414	55	19	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	414	55	19	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	668	415	139	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	722	415	139	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	665	415	139	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
482223	17:7675080-7675080	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	675	415	139	H/D	Cac/Gac	rs1064795203,CD983489,CM111332,COSV52693338,COSV52783253,COSV52816064	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	672	530	177	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	530	530	177	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	530	530	177	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	663	530	177	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	666	530	177	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	663	530	177	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=147;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	412	134	45	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	412	134	45	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	786	-	-	-	-	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=34;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	266	134	45	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	412	134	45	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	330	251	84	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	38	-	-	-	-	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1495;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=80;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	780	413	138	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	663	413	138	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	412	53	18	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	412	53	18	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	412	53	18	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	666	413	138	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	720	413	138	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	663	413	138	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
458547	17:7675082-7675082	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	673	413	138	P/R	cCc/cGc	rs751477326,CM102507,COSV52661381,COSV52721872,COSV52783879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	669-670	527-528	176	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	527-528	527-528	176	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	527-528	527-528	176	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	660-661	527-528	176	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	663-664	527-528	176	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	660-661	527-528	176	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52756284,COSV99037144,COSV99403879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=144;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	409-410	131-132	44	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	409-410	131-132	44	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	783-784	-	-	-	-	COSV52756284,COSV99037144,COSV99403879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52756284,COSV99037144,COSV99403879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=31;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	263-264	131-132	44	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	409-410	131-132	44	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	327-328	248-249	83	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	35-36	-	-	-	-	COSV52756284,COSV99037144,COSV99403879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52756284,COSV99037144,COSV99403879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1497;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52756284,COSV99037144,COSV99403879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=77;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	777-778	410-411	137	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	660-661	410-411	137	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	409-410	50-51	17	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	409-410	50-51	17	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	409-410	50-51	17	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	663-664	410-411	137	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	717-718	410-411	137	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	660-661	410-411	137	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1076864	17:7675084-7675084	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	670-671	410-411	137	C/CX	tgc/tgTc	COSV52756284,COSV99037144,COSV99403879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	670	528	176	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	528	528	176	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	528	528	176	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	661	528	176	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	664	528	176	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	661	528	176	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=145;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	410	132	44	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	410	132	44	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	784	-	-	-	-	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=32;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	264	132	44	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	410	132	44	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	328	249	83	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	36	-	-	-	-	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1497;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=78;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	778	411	137	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	661	411	137	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	410	51	17	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	410	51	17	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	410	51	17	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	664	411	137	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	718	411	137	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	661	411	137	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1746607	17:7675084-7675084	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	671	411	137	C/*	tgC/tgA	COSV52687391,COSV52701599,COSV52735850,COSV99377692	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	668-670	526-528	176	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	526-528	526-528	176	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	526-528	526-528	176	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	659-661	526-528	176	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	662-664	526-528	176	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	659-661	526-528	176	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=143;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	408-410	130-132	44	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	408-410	130-132	44	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	782-784	-	-	-	-	rs1567552847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=30;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	262-264	130-132	44	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	408-410	130-132	44	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	326-328	247-249	83	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	34-36	-	-	-	-	rs1567552847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567552847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1497;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=76;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	776-778	409-411	137	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	659-661	409-411	137	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	408-410	49-51	17	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	408-410	49-51	17	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	408-410	49-51	17	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	662-664	409-411	137	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	716-718	409-411	137	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	659-661	409-411	137	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634759	17:7675084-7675086	CCG	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	669-671	409-411	137	C/R	TGC/CGG	rs1567552847	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	669	527	176	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	527	527	176	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	527	527	176	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	660	527	176	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	663	527	176	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	660	527	176	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=144;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	409	131	44	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	409	131	44	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	783	-	-	-	-	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=31;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	263	131	44	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	409	131	44	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	327	248	83	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	35	-	-	-	-	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1498;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=77;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	777	410	137	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	660	410	137	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	409	50	17	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	409	50	17	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	409	50	17	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	663	410	137	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	717	410	137	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	660	410	137	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376569	17:7675085-7675085	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	670	410	137	C/F	tGc/tTc	rs786202962,COSV52660760,COSV52661329,COSV52678029	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	665	523	175	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	523	523	175	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	523	523	175	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	656	523	175	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	659	523	175	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	656	523	175	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=140;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	405	127	43	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	405	127	43	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	779	-	-	-	-	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=27;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	259	127	43	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	405	127	43	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	323	244	82	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	31	-	-	-	-	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1502;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=73;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	773	406	136	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	656	406	136	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	405	46	16	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	405	46	16	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	405	46	16	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	659	406	136	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	713	406	136	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	656	406	136	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376649	17:7675089-7675089	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	666	406	136	R/G	Cgc/Ggc	rs138729528,CM011013,CM118880,COSV52688031,COSV52713177,COSV52717943,COSV53372849	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	651-662	509-520	170-174	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	509-520	509-520	170-174	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	509-520	509-520	170-174	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	642-653	509-520	170-174	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	645-656	509-520	170-174	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	642-653	509-520	170-174	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=126;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	391-402	113-124	38-42	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	391-402	113-124	38-42	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	765-776	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=13;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	245-256	113-124	38-42	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	391-402	113-124	38-42	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000514944.5	Transcript	inframe_deletion	309-320	230-241	77-81	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	17-28	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1505;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=59;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	759-770	392-403	131-135	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	642-653	392-403	131-135	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000610623.4	Transcript	inframe_deletion	391-402	32-43	11-15	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000618944.4	Transcript	inframe_deletion	391-402	32-43	11-15	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000619186.4	Transcript	inframe_deletion	391-402	32-43	11-15	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	645-656	392-403	131-135	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	699-710	392-403	131-135	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	642-653	392-403	131-135	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1067825	17:7675091-7675103	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	652-663	392-403	131-135	TEVVR/R	aCGGAGGTTGTGAgg/agg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	660	518	173	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	518	518	173	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	518	518	173	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	651	518	173	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	654	518	173	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	651	518	173	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=135;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	400	122	41	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	400	122	41	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	774	-	-	-	-	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=22;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	254	122	41	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	400	122	41	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	318	239	80	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	26	-	-	-	-	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1507;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=68;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	768	401	134	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	651	401	134	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	400	41	14	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	400	41	14	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	400	41	14	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	654	401	134	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	708	401	134	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	651	401	134	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376017	17:7675094-7675094	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	661	401	134	V/A	gTg/gCg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	660	518	173	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	518	518	173	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	518	518	173	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	651	518	173	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	654	518	173	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	651	518	173	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=135;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	400	122	41	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	400	122	41	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	774	-	-	-	-	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=22;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	254	122	41	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	400	122	41	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	318	239	80	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	26	-	-	-	-	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1507;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=68;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	768	401	134	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	651	401	134	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	400	41	14	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	400	41	14	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	400	41	14	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	654	401	134	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	708	401	134	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	651	401	134	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376669	17:7675094-7675094	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	661	401	134	V/E	gTg/gAg	rs1057519747,COSV52679619,COSV52753659,COSV52782945	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	659-660	517-518	173	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	517-518	517-518	173	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	517-518	517-518	173	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	650-651	517-518	173	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	653-654	517-518	173	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	650-651	517-518	173	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=134;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	399-400	121-122	41	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	399-400	121-122	41	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	773-774	-	-	-	-	rs1555526064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=21;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	253-254	121-122	41	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	399-400	121-122	41	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	317-318	238-239	80	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	25-26	-	-	-	-	rs1555526064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1507;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526064	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=67;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	767-768	400-401	134	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	650-651	400-401	134	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	399-400	40-41	14	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	399-400	40-41	14	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	399-400	40-41	14	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	653-654	400-401	134	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	707-708	400-401	134	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	650-651	400-401	134	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
545786	17:7675094-7675094	CAAC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	660-661	400-401	134	V/GCX	gtg/gGTTGtg	rs1555526064	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	659	517	173	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	517	517	173	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	517	517	173	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	650	517	173	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	653	517	173	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	650	517	173	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=134;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	399	121	41	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	399	121	41	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	773	-	-	-	-	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=21;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	253	121	41	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	399	121	41	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	317	238	80	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	25	-	-	-	-	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1508;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=67;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	767	400	134	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	650	400	134	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	399	40	14	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	399	40	14	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	399	40	14	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	653	400	134	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	707	400	134	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	650	400	134	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
376668	17:7675095-7675095	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	660	400	134	V/L	Gtg/Ttg	rs876660754,CM070299,COSV52676535,COSV52677795,COSV52695723,COSV52823354	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	657-658	515-516	172	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	515-516	515-516	172	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	515-516	515-516	172	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	648-649	515-516	172	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	651-652	515-516	172	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	648-649	515-516	172	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=132;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	397-398	119-120	40	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	397-398	119-120	40	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	771-772	-	-	-	-	rs786202514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=19;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	251-252	119-120	40	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	397-398	119-120	40	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	315-316	236-237	79	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	23-24	-	-	-	-	rs786202514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1509;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=65;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	765-766	398-399	133	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	648-649	398-399	133	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	397-398	38-39	13	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	397-398	38-39	13	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	397-398	38-39	13	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	651-652	398-399	133	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	705-706	398-399	133	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	648-649	398-399	133	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
185860	17:7675096-7675096	ACCTC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	658-659	398-399	133	V/VRX	gtt/gtGAGGTt	rs786202514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	656	514	172	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	514	514	172	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	514	514	172	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	647	514	172	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	650	514	172	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	647	514	172	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=131;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	396	118	40	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	396	118	40	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	770	-	-	-	-	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=18;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	250	118	40	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	396	118	40	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	314	235	79	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	22	-	-	-	-	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1511;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=64;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	764	397	133	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	647	397	133	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	396	37	13	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	396	37	13	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	396	37	13	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	650	397	133	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	704	397	133	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	647	397	133	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
428909	17:7675098-7675098	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	657	397	133	V/F	Gtt/Ttt	rs1131691043,CM115637,COSV52672812,COSV52700410	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	651-654	509-512	170-171	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	509-512	509-512	170-171	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	509-512	509-512	170-171	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	642-645	509-512	170-171	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	645-648	509-512	170-171	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	642-645	509-512	170-171	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=126;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	391-394	113-116	38-39	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	391-394	113-116	38-39	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	765-768	-	-	-	-	rs1555526082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=13;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	245-248	113-116	38-39	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	391-394	113-116	38-39	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	309-312	230-233	77-78	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	17-20	-	-	-	-	rs1555526082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1513;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526082	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=59;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	759-762	392-395	131-132	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	642-645	392-395	131-132	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	391-394	32-35	11-12	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	391-394	32-35	11-12	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	391-394	32-35	11-12	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	645-648	392-395	131-132	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	699-702	392-395	131-132	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	642-645	392-395	131-132	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480750	17:7675099-7675103	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	652-655	392-395	131-132	TE/X	aCGGAg/ag	rs1555526082	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	654	512	171	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	512	512	171	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	512	512	171	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	645	512	171	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	648	512	171	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	645	512	171	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=129;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	394	116	39	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	394	116	39	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	768	-	-	-	-	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=16;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	248	116	39	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	394	116	39	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	312	233	78	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	20	-	-	-	-	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1513;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=62;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	762	395	132	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	645	395	132	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	394	35	12	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	394	35	12	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	394	35	12	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	648	395	132	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	702	395	132	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	645	395	132	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745525	17:7675100-7675100	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	655	395	132	E/G	gAg/gGg	CD098501,COSV52700191,COSV52740895,COSV53706637	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	653	511	171	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	511	511	171	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	511	511	171	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	644	511	171	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	647	511	171	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	644	511	171	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=128;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	393	115	39	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	393	115	39	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	767	-	-	-	-	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=15;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	247	115	39	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	393	115	39	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	311	232	78	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	19	-	-	-	-	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1514;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=61;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	761	394	132	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	644	394	132	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	393	34	12	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	393	34	12	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	393	34	12	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	647	394	132	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	701	394	132	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	644	394	132	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634771	17:7675101-7675101	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	654	394	132	E/*	Gag/Tag	rs587781845,COSV52671445,COSV52701260,COSV52703282	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	652-653	510-511	170-171	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	510-511	510-511	170-171	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	510-511	510-511	170-171	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	643-644	510-511	170-171	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	646-647	510-511	170-171	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	643-644	510-511	170-171	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597370110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=127;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	392-393	114-115	38-39	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	392-393	114-115	38-39	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	766-767	-	-	-	-	rs1597370110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597370110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	246-247	114-115	38-39	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	392-393	114-115	38-39	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	310-311	231-232	77-78	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	18-19	-	-	-	-	rs1597370110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597370110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1514;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597370110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=60;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	760-761	393-394	131-132	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	643-644	393-394	131-132	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	392-393	33-34	11-12	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	392-393	33-34	11-12	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	392-393	33-34	11-12	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	646-647	393-394	131-132	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	700-701	393-394	131-132	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	643-644	393-394	131-132	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
640351	17:7675101-7675101	CG	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	653-654	393-394	131-132	-/X	-/CG	rs1597370110	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	621-645	479-503	160-168	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	479-503	479-503	160-168	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	479-503	479-503	160-168	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	612-636	479-503	160-168	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	615-639	479-503	160-168	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	612-636	479-503	160-168	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=96;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	361-385	83-107	28-36	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	361-385	83-107	28-36	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	735-759	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000508793.5	Transcript	coding_sequence_variant,3_prime_UTR_variant	617-?	479-?	160-?	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	215-239	83-107	28-36	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	361-385	83-107	28-36	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	279-303	200-224	67-75	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	?-11	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1522;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=29;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	729-753	362-386	121-129	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	612-636	362-386	121-129	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant,start_lost	361-385	2-26	1-9	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant,start_lost	361-385	2-26	1-9	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant,start_lost	361-385	2-26	1-9	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	615-639	362-386	121-129	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	669-693	362-386	121-129	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	612-636	362-386	121-129	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1397281	17:7675108-7675133	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	622-646	362-386	121-129	MAIYKQSQH/X	aTGGCCATCTACAAGCAGTCACAGCAc/ac	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	645	503	168	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	503	503	168	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	503	503	168	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	636	503	168	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	639	503	168	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	636	503	168	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=120;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	385	107	36	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	385	107	36	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	759	-	-	-	-	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=7;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	239	107	36	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	385	107	36	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	303	224	75	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	11	-	-	-	-	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1522;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=53;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	753	386	129	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	636	386	129	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	385	26	9	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	385	26	9	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	385	26	9	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	639	386	129	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	693	386	129	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	636	386	129	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744933	17:7675109-7675109	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	646	386	129	H/L	cAc/cTc	COSV52676197,COSV52682212,COSV52698349,COSV52762255	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	643	501	167	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	501	501	167	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	501	501	167	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	634	501	167	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	637	501	167	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	634	501	167	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=118;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	383	105	35	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	383	105	35	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	757	-	-	-	-	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	237	105	35	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	383	105	35	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	301	222	74	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	9	-	-	-	-	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1524;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=51;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	751	384	128	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	634	384	128	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	383	24	8	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	383	24	8	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	383	24	8	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	637	384	128	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	691	384	128	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	634	384	128	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
566517	17:7675110-7675111	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	644	384	128	Q/X	caG/ca	rs1567553148,COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	641	499	167	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	499	499	167	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	499	499	167	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	632	499	167	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	635	499	167	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	632	499	167	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=116;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	381	103	35	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	381	103	35	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	755	-	-	-	-	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	235	103	35	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	381	103	35	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	299	220	74	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	7	-	-	-	-	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1526;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=49;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	749	382	128	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	632	382	128	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	381	22	8	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	381	22	8	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	381	22	8	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	635	382	128	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	689	382	128	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	632	382	128	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
528250	17:7675113-7675113	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	642	382	128	Q/*	Cag/Tag	rs1555526097,CM942118,COSV52735517,COSV53025177,COSV53136193,COSV53312374	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	639-640	497-498	166	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	497-498	497-498	166	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	497-498	497-498	166	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	630-631	497-498	166	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	633-634	497-498	166	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	630-631	497-498	166	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=114;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	379-380	101-102	34	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	379-380	101-102	34	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	753-754	-	-	-	-	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	233-234	101-102	34	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	379-380	101-102	34	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	297-298	218-219	73	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	5-6	-	-	-	-	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1527;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=47;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	747-748	380-381	127	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	630-631	380-381	127	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	379-380	20-21	7	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	379-380	20-21	7	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	379-380	20-21	7	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	633-634	380-381	127	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	687-688	380-381	127	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	630-631	380-381	127	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825196	17:7675114-7675114	GACTGCTTGTAGATGGC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	640-641	380-381	127	S/SPSTSSX	tca/tcGCCATCTACAAGCAGTCa	rs1597370230,COSV53059983,COSV53125131,COSV99444099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	639	497	166	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	497	497	166	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	497	497	166	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	630	497	166	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	633	497	166	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	630	497	166	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=114;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	379	101	34	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	379	101	34	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	753	-	-	-	-	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	233	101	34	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	379	101	34	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	297	218	73	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	5	-	-	-	-	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1528;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=47;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	747	380	127	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	630	380	127	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	379	20	7	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	379	20	7	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	379	20	7	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	633	380	127	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	687	380	127	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	630	380	127	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634699	17:7675115-7675115	C	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	640	380	127	S/*	tCa/tGa	rs1555526101,COSV52661795,COSV52683537,COSV52718793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	635	493	165	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	493	493	165	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	493	493	165	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	626	493	165	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	629	493	165	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	626	493	165	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=110;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	375	97	33	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	375	97	33	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	749	-	-	-	-	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	631	493	165	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	229	97	33	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	375	97	33	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	293	214	72	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	1	-	-	-	-	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1532;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=43;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	743	376	126	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	626	376	126	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	375	16	6	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	375	16	6	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	375	16	6	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	629	376	126	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	683	376	126	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	626	376	126	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
182930	17:7675119-7675119	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	636	376	126	Q/*	Cag/Tag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	634-635	492-493	164-165	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	492-493	492-493	164-165	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	492-493	492-493	164-165	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	625-626	492-493	164-165	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	628-629	492-493	164-165	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	625-626	492-493	164-165	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553215,COSV53715874	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=109;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	374-375	96-97	32-33	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	374-375	96-97	32-33	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	748-749	-	-	-	-	rs1567553215,COSV53715874	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	630-631	492-493	164-165	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	228-229	96-97	32-33	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	374-375	96-97	32-33	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	292-293	213-214	71-72	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	?-1	-	-	-	-	rs1567553215,COSV53715874	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553215,COSV53715874	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1532;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553215,COSV53715874	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=42;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	742-743	375-376	125-126	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	625-626	375-376	125-126	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	374-375	15-16	5-6	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	374-375	15-16	5-6	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	374-375	15-16	5-6	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	628-629	375-376	125-126	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	682-683	375-376	125-126	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	625-626	375-376	125-126	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
579699	17:7675119-7675120	AG	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	635-636	375-376	125-126	KQ/N*	aaGCag/aaCTag	rs1567553215,COSV53715874	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	632	490	164	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	490	490	164	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	490	490	164	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	623	490	164	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	626	490	164	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	623	490	164	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=107;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	372	94	32	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	372	94	32	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	746	-	-	-	-	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	628	490	164	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	226	94	32	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	372	94	32	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	290	211	71	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1535;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=40;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	740	373	125	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	623	373	125	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	372	13	5	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	372	13	5	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	372	13	5	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	626	373	125	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	680	373	125	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	623	373	125	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
935480	17:7675122-7675122	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	633	373	125	K/*	Aag/Tag	COSV52676020,COSV52700231,COSV52728094,COSV52766542	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	631	489	163	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	489	489	163	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	489	489	163	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	622	489	163	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	625	489	163	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	622	489	163	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=106;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	371	93	31	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	371	93	31	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	745	-	-	-	-	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	627	489	163	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	225	93	31	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	371	93	31	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	289	210	70	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1536;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=39;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	739	372	124	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	622	372	124	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	371	12	4	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	371	12	4	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	371	12	4	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	625	372	124	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	679	372	124	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	622	372	124	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1421837	17:7675123-7675123	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	632	372	124	Y/*	taC/taA	CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	630-631	488-489	163	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	488-489	488-489	163	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	488-489	488-489	163	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	621-622	488-489	163	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	624-625	488-489	163	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	621-622	488-489	163	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=105;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	370-371	92-93	31	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	370-371	92-93	31	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	744-745	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	626-627	488-489	163	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	224-225	92-93	31	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	370-371	92-93	31	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	288-289	209-210	70	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1536;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=38;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	738-739	371-372	124	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	621-622	371-372	124	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	370-371	11-12	4	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	370-371	11-12	4	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	370-371	11-12	4	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	624-625	371-372	124	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	678-679	371-372	124	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	621-622	371-372	124	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1743576	17:7675123-7675123	TAGA	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	631-632	371-372	124	Y/YLX	tac/taTCTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	631	489	163	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	489	489	163	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	489	489	163	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	622	489	163	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	625	489	163	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	622	489	163	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=106;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	371	93	31	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	371	93	31	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	745	-	-	-	-	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	627	489	163	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	225	93	31	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	371	93	31	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	289	210	70	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1536;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=39;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	739	372	124	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	622	372	124	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	371	12	4	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000618944.4	Transcript	stop_gained	371	12	4	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000619186.4	Transcript	stop_gained	371	12	4	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	625	372	124	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	679	372	124	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	622	372	124	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
619734	17:7675123-7675123	C	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	632	372	124	Y/*	taC/taG	rs1567553246,CM167569,COSV52741368,COSV52741580,COSV52875770,COSV53211332	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	628-631	486-489	162-163	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	486-489	486-489	162-163	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	486-489	486-489	162-163	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	619-622	486-489	162-163	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	622-625	486-489	162-163	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	619-622	486-489	162-163	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597370312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=103;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	368-371	90-93	30-31	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	368-371	90-93	30-31	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	742-745	-	-	-	-	rs1597370312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	624-627	486-489	162-163	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	222-225	90-93	30-31	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	368-371	90-93	30-31	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	286-289	207-210	69-70	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597370312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597370312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1536;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597370312	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=36;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	736-739	369-372	123-124	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	619-622	369-372	123-124	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	368-371	9-12	3-4	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	368-371	9-12	3-4	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	368-371	9-12	3-4	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	622-625	369-372	123-124	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	676-679	369-372	123-124	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	619-622	369-372	123-124	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
825238	17:7675123-7675126	ACAAGCAGTCTACA	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	629-632	369-372	123-124	IY/IVDCLX	atCTAC/atTGTAGACTGCTTGT	rs1597370312	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	623-624	481-482	161	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	481-482	481-482	161	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	481-482	481-482	161	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	614-615	481-482	161	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	617-618	481-482	161	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	614-615	481-482	161	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs863223301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=98;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	363-364	85-86	29	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	363-364	85-86	29	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	737-738	-	-	-	-	rs863223301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	619-620	481-482	161	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	217-218	85-86	29	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	363-364	85-86	29	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	281-282	202-203	68	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs863223301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs863223301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1543;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863223301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=31;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	731-732	364-365	122	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	614-615	364-365	122	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant	363-364	4-5	2	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000618944.4	Transcript	frameshift_variant	363-364	4-5	2	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000619186.4	Transcript	frameshift_variant	363-364	4-5	2	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	617-618	364-365	122	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	671-672	364-365	122	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	614-615	364-365	122	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
12380	17:7675130-7675130	CCATGGC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	624-625	364-365	122	A/GHGX	gcc/gGCCATGGcc	rs863223301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	611-618	469-476	157-159	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	469-476	469-476	157-159	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	469-476	469-476	157-159	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	602-609	469-476	157-159	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	605-612	469-476	157-159	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	602-609	469-476	157-159	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=86;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	351-358	73-80	25-27	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	351-358	73-80	25-27	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	725-732	-	-	-	-	rs1555526137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	607-614	469-476	157-159	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	205-212	73-80	25-27	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	351-358	73-80	25-27	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	269-276	190-197	64-66	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=17;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1549;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=19;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	719-726	352-359	118-120	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	602-609	352-359	118-120	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	351-358	-	-	-	-	rs1555526137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	351-358	-	-	-	-	rs1555526137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	351-358	-	-	-	-	rs1555526137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	605-612	352-359	118-120	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	659-666	352-359	118-120	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	602-609	352-359	118-120	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492750	17:7675135-7675143	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	612-619	352-359	118-120	VRA/X	GTCCGCGCc/c	rs1555526137	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	613-616	471-474	157-158	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	471-474	471-474	157-158	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	471-474	471-474	157-158	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	604-607	471-474	157-158	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	607-610	471-474	157-158	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	604-607	471-474	157-158	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=88;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	353-356	75-78	25-26	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	353-356	75-78	25-26	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	727-730	-	-	-	-	rs1567553514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	609-612	471-474	157-158	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	207-210	75-78	25-26	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	353-356	75-78	25-26	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	271-274	192-195	64-65	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=19;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1551;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=21;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	721-724	354-357	118-119	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	604-607	354-357	118-119	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	353-356	-	-	-	-	rs1567553514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	353-356	-	-	-	-	rs1567553514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	353-356	-	-	-	-	rs1567553514	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	607-610	354-357	118-119	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	661-664	354-357	118-119	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	604-607	354-357	118-119	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634760	17:7675137-7675141	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	614-617	354-357	118-119	VR/X	gtCCGC/gt	rs1567553514	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	615-616	473-474	158	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	473-474	473-474	158	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	473-474	473-474	158	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	606-607	473-474	158	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	609-610	473-474	158	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	606-607	473-474	158	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553501,COSV52979130	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=90;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	355-356	77-78	26	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	355-356	77-78	26	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	729-730	-	-	-	-	rs1567553501,COSV52979130	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	611-612	473-474	158	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	209-210	77-78	26	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	355-356	77-78	26	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	273-274	194-195	65	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553501,COSV52979130	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=19;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553501,COSV52979130	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1551;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553501,COSV52979130	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=23;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	723-724	356-357	119	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	606-607	356-357	119	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	355-356	-	-	-	-	rs1567553501,COSV52979130	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	355-356	-	-	-	-	rs1567553501,COSV52979130	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	355-356	-	-	-	-	rs1567553501,COSV52979130	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	609-610	356-357	119	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	663-664	356-357	119	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	606-607	356-357	119	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
568285	17:7675138-7675139	AA	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	616-617	356-357	119	R/L	cGC/cTT	rs1567553501,COSV52979130	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	615	473	158	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	473	473	158	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	473	473	158	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	606	473	158	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	609	473	158	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	606	473	158	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=90;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	355	77	26	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	355	77	26	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	729	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	611	473	158	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	209	77	26	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	355	77	26	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	273	194	65	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=20;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1552;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=23;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	723	356	119	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	606	356	119	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	355	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	355	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	355	-	-	-	-	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	609	356	119	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	663	356	119	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	606	356	119	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
528248	17:7675139-7675139	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	616	356	119	R/L	cGc/cTc	rs587782144,CM102353,CM165595,CM994513,COSV52676395,COSV52678258,COSV52680378,COSV53545833	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	614	472	158	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	472	472	158	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	472	472	158	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	605	472	158	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	608	472	158	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	605	472	158	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=89;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	354	76	26	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	354	76	26	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	728	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	610	472	158	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	208	76	26	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	354	76	26	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	272	193	65	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=21;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1553;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=22;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	722	355	119	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	605	355	119	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	354	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	354	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	354	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	608	355	119	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	662	355	119	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	605	355	119	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1067910	17:7675140-7675140	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	615	355	119	R/S	Cgc/Agc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	614	472	158	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	472	472	158	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	472	472	158	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	605	472	158	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	608	472	158	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	605	472	158	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=89;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	354	76	26	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	354	76	26	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	728	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	610	472	158	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	208	76	26	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	354	76	26	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	272	193	65	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=21;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1553;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=22;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	722	355	119	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	605	355	119	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	354	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	354	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	354	-	-	-	-	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	608	355	119	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	662	355	119	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	605	355	119	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
856171	17:7675140-7675140	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	615	355	119	R/G	Cgc/Ggc	CM004341,CM121763,COSV52677865,COSV52699654,COSV52778687	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	612	470	157	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	470	470	157	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	470	470	157	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	603	470	157	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	606	470	157	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	603	470	157	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=87;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	352	74	25	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	352	74	25	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	726	-	-	-	-	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	608	470	157	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	206	74	25	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	352	74	25	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	270	191	64	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=23;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1555;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=20;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	720	353	118	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	603	353	118	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	352	-	-	-	-	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	352	-	-	-	-	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	352	-	-	-	-	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	606	353	118	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	660	353	118	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	603	353	118	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428887	17:7675142-7675142	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	613	353	118	V/A	gTc/gCc	rs1131691023,CM138009,CM161671,COSV52675572,COSV52699845,COSV52722122	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	596-608	454-466	152-156	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	454-466	454-466	152-156	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	454-466	454-466	152-156	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	587-599	454-466	152-156	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	590-602	454-466	152-156	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	587-599	454-466	152-156	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=71;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	336-348	58-70	20-24	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	336-348	58-70	20-24	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	710-722	-	-	-	-	rs876659215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	592-604	454-466	152-156	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	190-202	58-70	20-24	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	336-348	58-70	20-24	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	254-266	175-187	59-63	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=27;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1559;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	704-716	337-349	113-117	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	587-599	337-349	113-117	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	336-348	-	-	-	-	rs876659215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	336-348	-	-	-	-	rs876659215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	336-348	-	-	-	-	rs876659215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	590-602	337-349	113-117	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	644-656	337-349	113-117	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	587-599	337-349	113-117	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
231540	17:7675145-7675158	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	597-609	337-349	113-117	PPGTR/X	CCGCCCGGCACCCgc/gc	rs876659215	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	600-608	458-466	153-156	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	458-466	458-466	153-156	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	458-466	458-466	153-156	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	591-599	458-466	153-156	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	594-602	458-466	153-156	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	591-599	458-466	153-156	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=75;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	340-348	62-70	21-24	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	340-348	62-70	21-24	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	714-722	-	-	-	-	rs1567553613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000508793.5	Transcript	inframe_deletion	596-604	458-466	153-156	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	194-202	62-70	21-24	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	340-348	62-70	21-24	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000514944.5	Transcript	inframe_deletion	258-266	179-187	60-63	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=27;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1559;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=8;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	708-716	341-349	114-117	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	591-599	341-349	114-117	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	340-348	-	-	-	-	rs1567553613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	340-348	-	-	-	-	rs1567553613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	340-348	-	-	-	-	rs1567553613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	594-602	341-349	114-117	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	648-656	341-349	114-117	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	591-599	341-349	114-117	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634662	17:7675145-7675154	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	601-609	341-349	114-117	PGTR/R	cCCGGCACCCgc/cgc	rs1567553613	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	602-605	460-463	154-155	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	460-463	460-463	154-155	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	460-463	460-463	154-155	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	593-596	460-463	154-155	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	596-599	460-463	154-155	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	593-596	460-463	154-155	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=77;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	342-345	64-67	22-23	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	342-345	64-67	22-23	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	716-719	-	-	-	-	rs1567553658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	598-601	460-463	154-155	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	196-199	64-67	22-23	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	342-345	64-67	22-23	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	260-263	181-184	61-62	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=30;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1562;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=10;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	710-713	343-346	115-116	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	593-596	343-346	115-116	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	342-345	-	-	-	-	rs1567553658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	342-345	-	-	-	-	rs1567553658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	342-345	-	-	-	-	rs1567553658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	596-599	343-346	115-116	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	650-653	343-346	115-116	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	593-596	343-346	115-116	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634666	17:7675148-7675152	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	603-606	343-346	115-116	GT/X	GGCAcc/cc	rs1567553658	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	604-605	462-463	154-155	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	462-463	462-463	154-155	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	462-463	462-463	154-155	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	595-596	462-463	154-155	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	598-599	462-463	154-155	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	595-596	462-463	154-155	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=79;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	344-345	66-67	22-23	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	344-345	66-67	22-23	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	718-719	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	600-601	462-463	154-155	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	198-199	66-67	22-23	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	344-345	66-67	22-23	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	262-263	183-184	61-62	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=30;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1562;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=12;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	712-713	345-346	115-116	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	595-596	345-346	115-116	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	344-345	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	344-345	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	344-345	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	598-599	345-346	115-116	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	652-653	345-346	115-116	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	595-596	345-346	115-116	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1073670	17:7675149-7675149	GCCGG	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	605-606	345-346	115-116	-/PX	-/CCGGC	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	590-602	448-460	150-154	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	448-460	448-460	150-154	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	448-460	448-460	150-154	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	581-593	448-460	150-154	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	584-596	448-460	150-154	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	581-593	448-460	150-154	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064792930,COSV52702198	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=65;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	330-342	52-64	18-22	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	330-342	52-64	18-22	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	704-716	-	-	-	-	rs1064792930,COSV52702198	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	586-598	448-460	150-154	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	184-196	52-64	18-22	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	330-342	52-64	18-22	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	248-260	169-181	57-61	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064792930,COSV52702198	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=33;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064792930,COSV52702198	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1565;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000604348.5	Transcript	coding_sequence_variant,3_prime_UTR_variant	566-?	427-?	143-?	-	-	rs1064792930,COSV52702198	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	698-710	331-343	111-115	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	581-593	331-343	111-115	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	330-342	-	-	-	-	rs1064792930,COSV52702198	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	330-342	-	-	-	-	rs1064792930,COSV52702198	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	330-342	-	-	-	-	rs1064792930,COSV52702198	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	584-596	331-343	111-115	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	638-650	331-343	111-115	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	581-593	331-343	111-115	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
406602	17:7675151-7675164	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	591-603	331-343	111-115	TPPPG/X	ACACCCCCGCCCGgc/gc	rs1064792930,COSV52702198	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000269305.9	Transcript	inframe_insertion	602-603	460-461	154	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000359597.8	Transcript	inframe_insertion	460-461	460-461	154	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000413465.6	Transcript	inframe_insertion	460-461	460-461	154	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000420246.6	Transcript	inframe_insertion	593-594	460-461	154	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000445888.6	Transcript	inframe_insertion	596-597	460-461	154	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000455263.6	Transcript	inframe_insertion	593-594	460-461	154	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553717,COSV53792382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=77;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000504290.5	Transcript	inframe_insertion	342-343	64-65	22	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000504937.5	Transcript	inframe_insertion	342-343	64-65	22	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	716-717	-	-	-	-	rs1567553717,COSV53792382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000508793.5	Transcript	inframe_insertion	598-599	460-461	154	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000509690.5	Transcript	inframe_insertion	196-197	64-65	22	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000510385.5	Transcript	inframe_insertion	342-343	64-65	22	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000514944.5	Transcript	inframe_insertion	260-261	181-182	61	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553717,COSV53792382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=32;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553717,COSV53792382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1564;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553717,COSV53792382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=10;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000610292.4	Transcript	inframe_insertion	710-711	343-344	115	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000610538.4	Transcript	inframe_insertion	593-594	343-344	115	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	342-343	-	-	-	-	rs1567553717,COSV53792382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	342-343	-	-	-	-	rs1567553717,COSV53792382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	342-343	-	-	-	-	rs1567553717,COSV53792382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000619485.4	Transcript	inframe_insertion	596-597	343-344	115	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000620739.4	Transcript	inframe_insertion	650-651	343-344	115	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000622645.4	Transcript	inframe_insertion	593-594	343-344	115	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
634660	17:7675151-7675151	CGGGCGGGGGTGTGGAAT	ENSG00000141510	ENST00000635293.1	Transcript	inframe_insertion,NMD_transcript_variant	603-604	343-344	115	G/DSTPPPG	ggc/gATTCCACACCCCCGCCCGgc	rs1567553717,COSV53792382	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	589-601	447-459	149-153	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	447-459	447-459	149-153	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	447-459	447-459	149-153	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	580-592	447-459	149-153	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	583-595	447-459	149-153	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	580-592	447-459	149-153	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs137852790	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=64;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	329-341	51-63	17-21	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	329-341	51-63	17-21	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	703-715	-	-	-	-	rs137852790	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	585-597	447-459	149-153	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	183-195	51-63	17-21	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	329-341	51-63	17-21	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	247-259	168-180	56-60	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs137852790	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=34;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs137852790	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1566;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000604348.5	Transcript	coding_sequence_variant,3_prime_UTR_variant	565-?	426-?	142-?	-	-	rs137852790	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	697-709	330-342	110-114	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	580-592	330-342	110-114	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	329-341	-	-	-	-	rs137852790	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	329-341	-	-	-	-	rs137852790	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	329-341	-	-	-	-	rs137852790	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	583-595	330-342	110-114	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	637-649	330-342	110-114	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	580-592	330-342	110-114	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
142337	17:7675152-7675165	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	590-602	330-342	110-114	STPPP/X	tcCACACCCCCGCCC/tc	rs137852790	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,pathogenic;PHENO=1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	597-598	455-456	152	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	455-456	455-456	152	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	455-456	455-456	152	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	588-589	455-456	152	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	591-592	455-456	152	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	588-589	455-456	152	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=72;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	337-338	59-60	20	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	337-338	59-60	20	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	711-712	-	-	-	-	COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	593-594	455-456	152	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	191-192	59-60	20	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	337-338	59-60	20	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	255-256	176-177	59	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=37;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1569;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	705-706	338-339	113	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	588-589	338-339	113	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	337-338	-	-	-	-	COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	337-338	-	-	-	-	COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	337-338	-	-	-	-	COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	591-592	338-339	113	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	645-646	338-339	113	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	588-589	338-339	113	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1741437	17:7675156-7675156	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	598-599	338-339	113	P/PX	ccg/ccTg	COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	597-598	455-456	152	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	455-456	455-456	152	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	455-456	455-456	152	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	588-589	455-456	152	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	591-592	455-456	152	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	588-589	455-456	152	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882019,COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=72;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	337-338	59-60	20	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	337-338	59-60	20	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	711-712	-	-	-	-	rs730882019,COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	593-594	455-456	152	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	191-192	59-60	20	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	337-338	59-60	20	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	255-256	176-177	59	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882019,COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=37;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882019,COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1569;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882019,COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	705-706	338-339	113	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	588-589	338-339	113	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	337-338	-	-	-	-	rs730882019,COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	337-338	-	-	-	-	rs730882019,COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	337-338	-	-	-	-	rs730882019,COSV53468298,COSV99394349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	591-592	338-339	113	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	645-646	338-339	113	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	588-589	338-339	113	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
182958	17:7675156-7675156	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	598-599	338-339	113	P/PX	ccg/ccCg	rs730882019,COSV53468298,COSV99394349	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	597	455	152	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	455	455	152	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	455	455	152	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	588	455	152	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	591	455	152	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	588	455	152	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=72;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	337	59	20	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	337	59	20	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	711	-	-	-	-	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	593	455	152	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	191	59	20	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	337	59	20	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	255	176	59	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=38;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1570;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	705	338	113	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	588	338	113	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	337	-	-	-	-	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	337	-	-	-	-	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	337	-	-	-	-	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	591	338	113	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	645	338	113	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	588	338	113	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
634779	17:7675156-7675157	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	598	338	113	P/X	cCg/cg	rs730882019,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	597	455	152	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	455	455	152	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	455	455	152	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	588	455	152	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	591	455	152	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	588	455	152	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=72;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	337	59	20	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	337	59	20	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	711	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	593	455	152	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	191	59	20	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	337	59	20	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	255	176	59	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=38;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1570;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	705	338	113	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	588	338	113	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	337	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	337	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	337	-	-	-	-	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	591	338	113	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	645	338	113	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	588	338	113	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
824998	17:7675157-7675157	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	598	338	113	P/R	cCg/cGg	rs587782705,CD147772,CM941327,COSV52666949,COSV52773466,COSV53038279	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	594	452	151	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	452	452	151	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	452	452	151	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	585	452	151	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	588	452	151	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	585	452	151	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=69;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	334	56	19	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	334	56	19	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	708	-	-	-	-	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	590	452	151	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	188	56	19	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	334	56	19	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	252	173	58	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=41;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1573;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	702	335	112	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	585	335	112	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	334	-	-	-	-	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	334	-	-	-	-	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	334	-	-	-	-	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	588	335	112	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	642	335	112	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	585	335	112	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376640	17:7675160-7675160	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	595	335	112	P/R	cCc/cGc	rs1057520000,COSV52677206,COSV52707835,COSV52811105	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	592-594	450-452	150-151	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	450-452	450-452	150-151	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	450-452	450-452	150-151	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	583-585	450-452	150-151	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	586-588	450-452	150-151	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	583-585	450-452	150-151	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=67;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	332-334	54-56	18-19	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	332-334	54-56	18-19	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	706-708	-	-	-	-	rs1567553834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	588-590	450-452	150-151	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	186-188	54-56	18-19	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	332-334	54-56	18-19	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	250-252	171-173	57-58	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=41;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1573;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000604348.5	Transcript	coding_sequence_variant,3_prime_UTR_variant	568-?	429-?	143-?	-	-	rs1567553834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	700-702	333-335	111-112	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	583-585	333-335	111-112	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	332-334	-	-	-	-	rs1567553834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	332-334	-	-	-	-	rs1567553834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	332-334	-	-	-	-	rs1567553834	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	586-588	333-335	111-112	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	640-642	333-335	111-112	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	583-585	333-335	111-112	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634789	17:7675160-7675162	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	593-595	333-335	111-112	TP/TX	acACCc/acTc	rs1567553834	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	593-594	451-452	151	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	451-452	451-452	151	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	451-452	451-452	151	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	584-585	451-452	151	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	587-588	451-452	151	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	584-585	451-452	151	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=68;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	333-334	55-56	19	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	333-334	55-56	19	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	707-708	-	-	-	-	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	589-590	451-452	151	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	187-188	55-56	19	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	333-334	55-56	19	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	251-252	172-173	58	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=41;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1573;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	701-702	334-335	112	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	584-585	334-335	112	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	333-334	-	-	-	-	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	333-334	-	-	-	-	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	333-334	-	-	-	-	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	587-588	334-335	112	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	641-642	334-335	112	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	584-585	334-335	112	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
824960	17:7675160-7675161	AA	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	594-595	334-335	112	P/F	CCc/TTc	rs1597370899,COSV52701496,COSV52948561	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	593	451	151	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	451	451	151	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	451	451	151	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	584	451	151	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	587	451	151	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	584	451	151	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=68;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	333	55	19	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	333	55	19	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	707	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	589	451	151	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	187	55	19	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	333	55	19	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	251	172	58	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=42;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1574;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	701	334	112	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	584	334	112	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	333	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	333	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	333	-	-	-	-	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	587	334	112	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	641	334	112	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	584	334	112	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376641	17:7675161-7675161	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	594	334	112	P/A	Ccc/Gcc	rs28934874,CM012662,CM120847,CM941326,COSV52661698,COSV52676321,COSV52676982,COSV52701855	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	587	445	149	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	445	445	149	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	445	445	149	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	578	445	149	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	581	445	149	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	578	445	149	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064793929,COSV52688587,COSV52700895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=62;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	327	49	17	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	327	49	17	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	701	-	-	-	-	rs1064793929,COSV52688587,COSV52700895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	583	445	149	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	181	49	17	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	327	49	17	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	245	166	56	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064793929,COSV52688587,COSV52700895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=48;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064793929,COSV52688587,COSV52700895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1580;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	563	424	142	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	695	328	110	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	578	328	110	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	327	-	-	-	-	rs1064793929,COSV52688587,COSV52700895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	327	-	-	-	-	rs1064793929,COSV52688587,COSV52700895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	327	-	-	-	-	rs1064793929,COSV52688587,COSV52700895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	581	328	110	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	635	328	110	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	578	328	110	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
419519	17:7675166-7675167	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	588	328	110	S/X	Tcc/cc	rs1064793929,COSV52688587,COSV52700895	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	587-588	445-446	149	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	445-446	445-446	149	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	445-446	445-446	149	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	578-579	445-446	149	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	581-582	445-446	149	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	578-579	445-446	149	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064793929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=62;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	327-328	49-50	17	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	327-328	49-50	17	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	701-702	-	-	-	-	rs1064793929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	583-584	445-446	149	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	181-182	49-50	17	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	327-328	49-50	17	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	245-246	166-167	56	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064793929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=47;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064793929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1579;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	563-564	424-425	142	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	695-696	328-329	110	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	578-579	328-329	110	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	327-328	-	-	-	-	rs1064793929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	327-328	-	-	-	-	rs1064793929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	327-328	-	-	-	-	rs1064793929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	581-582	328-329	110	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	635-636	328-329	110	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	578-579	328-329	110	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634706	17:7675166-7675166	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	588-589	328-329	110	S/FX	tcc/tTcc	rs1064793929	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	581	439	147	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	439	439	147	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	439	439	147	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	572	439	147	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	575	439	147	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	572	439	147	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567553924,COSV52675604,COSV52980910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=56;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	321	43	15	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	321	43	15	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	695	-	-	-	-	rs1567553924,COSV52675604,COSV52980910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	577	439	147	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	175	43	15	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	321	43	15	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	239	160	54	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553924,COSV52675604,COSV52980910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=54;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567553924,COSV52675604,COSV52980910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1586;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	557	418	140	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	689	322	108	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	572	322	108	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	321	-	-	-	-	rs1567553924,COSV52675604,COSV52980910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	321	-	-	-	-	rs1567553924,COSV52675604,COSV52980910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	321	-	-	-	-	rs1567553924,COSV52675604,COSV52980910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	575	322	108	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	629	322	108	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	572	322	108	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634668	17:7675172-7675173	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	582	322	108	V/X	Gtt/tt	rs1567553924,COSV52675604,COSV52980910	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	580	438	146	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	438	438	146	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	438	438	146	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	571	438	146	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	574	438	146	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	571	438	146	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=55;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	320	42	14	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	320	42	14	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	694	-	-	-	-	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	576	438	146	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	174	42	14	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	320	42	14	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	238	159	53	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=55;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1587;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	556	417	139	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	688	321	107	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	571	321	107	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	320	-	-	-	-	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	320	-	-	-	-	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	320	-	-	-	-	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	574	321	107	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	628	321	107	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	571	321	107	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428890	17:7675174-7675174	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	581	321	107	W/*	tgG/tgA	rs1131691026,CM101750,COSV52661500,COSV52987374,COSV53571745	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	579	437	146	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	437	437	146	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	437	437	146	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	570	437	146	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	573	437	146	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	570	437	146	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=54;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	319	41	14	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	319	41	14	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	693	-	-	-	-	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	575	437	146	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	173	41	14	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	319	41	14	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	237	158	53	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=56;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1588;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	555	416	139	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	687	320	107	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	570	320	107	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	319	-	-	-	-	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	319	-	-	-	-	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	319	-	-	-	-	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	573	320	107	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	627	320	107	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	570	320	107	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634785	17:7675175-7675175	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	580	320	107	W/*	tGg/tAg	rs1206165503,CM107391,COSV52661900,COSV52703354,COSV52753201	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	576	434	145	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	434	434	145	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	434	434	145	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	567	434	145	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	570	434	145	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	567	434	145	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=51;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	316	38	13	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	316	38	13	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	690	-	-	-	-	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	572	434	145	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	170	38	13	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	316	38	13	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	234	155	52	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=59;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1591;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	552	413	138	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	684	317	106	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	567	317	106	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	316	-	-	-	-	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	316	-	-	-	-	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	316	-	-	-	-	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	570	317	106	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	624	317	106	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	567	317	106	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480760	17:7675178-7675178	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	577	317	106	L/Q	cTg/cAg	rs587782197,COSV52676080,COSV52724970,COSV52728973	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	573-575	431-433	144-145	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	431-433	431-433	144-145	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	431-433	431-433	144-145	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	564-566	431-433	144-145	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	567-569	431-433	144-145	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	564-566	431-433	144-145	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=48;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	313-315	35-37	12-13	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	313-315	35-37	12-13	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	687-689	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000508793.5	Transcript	inframe_deletion	569-571	431-433	144-145	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	167-169	35-37	12-13	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	313-315	35-37	12-13	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000514944.5	Transcript	inframe_deletion	231-233	152-154	51-52	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=60;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1592;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000604348.5	Transcript	inframe_deletion	549-551	410-412	137-138	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	681-683	314-316	105-106	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	564-566	314-316	105-106	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	313-315	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	313-315	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	313-315	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	567-569	314-316	105-106	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	621-623	314-316	105-106	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	564-566	314-316	105-106	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
984967	17:7675178-7675181	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	574-576	314-316	105-106	QL/L	cAGCtg/ctg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	562-573	420-431	140-144	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	420-431	420-431	140-144	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	420-431	420-431	140-144	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	553-564	420-431	140-144	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	556-567	420-431	140-144	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	553-564	420-431	140-144	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV104581680	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=37;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	302-313	24-35	8-12	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000504937.5	Transcript	inframe_deletion	302-313	24-35	8-12	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	676-687	-	-	-	-	COSV104581680	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000508793.5	Transcript	inframe_deletion	558-569	420-431	140-144	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000509690.5	Transcript	inframe_deletion	156-167	24-35	8-12	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000510385.5	Transcript	inframe_deletion	302-313	24-35	8-12	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000514944.5	Transcript	inframe_deletion	220-231	141-152	47-51	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104581680	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=62;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104581680	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1594;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000604348.5	Transcript	inframe_deletion	538-549	399-410	133-137	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	670-681	303-314	101-105	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	553-564	303-314	101-105	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	302-313	-	-	-	-	COSV104581680	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	302-313	-	-	-	-	COSV104581680	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	302-313	-	-	-	-	COSV104581680	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	556-567	303-314	101-105	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	610-621	303-314	101-105	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	553-564	303-314	101-105	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1879359	17:7675180-7675192	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	563-574	303-314	101-105	TCPVQ/T	acCTGCCCTGTGCAg/acg	COSV104581680	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	572	430	144	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	430	430	144	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	430	430	144	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	563	430	144	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	566	430	144	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	563	430	144	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=47;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	312	34	12	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	312	34	12	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	686	-	-	-	-	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	568	430	144	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	166	34	12	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	312	34	12	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	230	151	51	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=63;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1595;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	548	409	137	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	680	313	105	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	563	313	105	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	312	-	-	-	-	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	312	-	-	-	-	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	312	-	-	-	-	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	566	313	105	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	620	313	105	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	563	313	105	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739616	17:7675181-7675182	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	573	313	105	Q/X	Cag/ag	CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	572-573	430-431	144	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	430-431	430-431	144	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	430-431	430-431	144	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	563-564	430-431	144	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	566-567	430-431	144	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	563-564	430-431	144	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99037288	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=47;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	312-313	34-35	12	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	312-313	34-35	12	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	686-687	-	-	-	-	COSV99037288	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	568-569	430-431	144	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	166-167	34-35	12	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	312-313	34-35	12	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	230-231	151-152	51	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99037288	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=62;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99037288	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1594;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	548-549	409-410	137	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	680-681	313-314	105	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	563-564	313-314	105	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	312-313	-	-	-	-	COSV99037288	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	312-313	-	-	-	-	COSV99037288	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	312-313	-	-	-	-	COSV99037288	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	566-567	313-314	105	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	620-621	313-314	105	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	563-564	313-314	105	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1739617	17:7675181-7675181	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	573-574	313-314	105	Q/PX	cag/cCag	COSV99037288	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	572	430	144	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	430	430	144	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	430	430	144	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	563	430	144	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	566	430	144	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	563	430	144	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=47;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	312	34	12	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	312	34	12	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	686	-	-	-	-	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	568	430	144	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	166	34	12	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	312	34	12	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	230	151	51	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=63;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1595;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	548	409	137	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	680	313	105	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	563	313	105	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	312	-	-	-	-	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	312	-	-	-	-	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	312	-	-	-	-	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	566	313	105	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	620	313	105	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	563	313	105	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634688	17:7675182-7675182	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	573	313	105	Q/*	Cag/Tag	rs757274881,CM102352,COSV52662339,COSV52764890,COSV53424649	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	560-569	418-427	140-143	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	418-427	418-427	140-143	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	418-427	418-427	140-143	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	551-560	418-427	140-143	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	554-563	418-427	140-143	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	551-560	418-427	140-143	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=35;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	300-309	22-31	8-11	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	300-309	22-31	8-11	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	674-683	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	556-565	418-427	140-143	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	154-163	22-31	8-11	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	300-309	22-31	8-11	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	218-227	139-148	47-50	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=66;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1598;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	536-545	397-406	133-136	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	668-677	301-310	101-104	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	551-560	301-310	101-104	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	300-309	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	300-309	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	300-309	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	554-563	301-310	101-104	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	608-617	301-310	101-104	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	551-560	301-310	101-104	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1738495	17:7675184-7675194	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	561-570	301-310	101-104	TCPV/X	ACCTGCCCTGtg/tg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	570	428	143	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	428	428	143	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	428	428	143	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	561	428	143	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	564	428	143	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	561	428	143	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=45;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	310	32	11	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	310	32	11	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	684	-	-	-	-	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	566	428	143	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	164	32	11	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	310	32	11	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	228	149	50	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=65;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1597;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	546	407	136	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	678	311	104	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	561	311	104	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	310	-	-	-	-	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	310	-	-	-	-	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	310	-	-	-	-	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	564	311	104	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	618	311	104	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	561	311	104	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
804214	17:7675184-7675184	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	571	311	104	V/A	gTg/gCg	rs1555526241,CM1511132,COSV52737174,COSV52760297,COSV52868891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	532-568	390-426	130-142	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	390-426	390-426	130-142	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	390-426	390-426	130-142	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	523-559	390-426	130-142	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	526-562	390-426	130-142	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	523-559	390-426	130-142	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597371154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=7;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000504290.5	Transcript	start_lost,5_prime_UTR_variant	272-308	?-30	?-10	-	-	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000504937.5	Transcript	start_lost,5_prime_UTR_variant	272-308	?-30	?-10	-	-	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	646-682	-	-	-	-	rs1597371154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	528-564	390-426	130-142	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000509690.5	Transcript	start_lost,5_prime_UTR_variant	126-162	?-30	?-10	-	-	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000510385.5	Transcript	start_lost,5_prime_UTR_variant	272-308	?-30	?-10	-	-	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	190-226	111-147	37-49	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597371154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=67;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597371154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1599;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-544	?-405	?-135	-	-	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	640-676	273-309	91-103	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	523-559	273-309	91-103	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	272-308	-	-	-	-	rs1597371154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	272-308	-	-	-	-	rs1597371154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	272-308	-	-	-	-	rs1597371154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	526-562	273-309	91-103	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	580-616	273-309	91-103	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	523-559	273-309	91-103	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824362	17:7675185-7675222	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	533-569	273-309	91-103	LNKMFCQLAKTCP/X	ctCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT/ct	rs1597371154	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	567	425	142	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	425	425	142	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	425	425	142	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	558	425	142	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	561	425	142	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	558	425	142	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52675441,COSV52815950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=42;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	307	29	10	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	307	29	10	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	681	-	-	-	-	COSV52675441,COSV52815950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	563	425	142	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	161	29	10	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	307	29	10	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	225	146	49	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52675441,COSV52815950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=68;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52675441,COSV52815950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1600;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	543	404	135	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	675	308	103	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	558	308	103	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	307	-	-	-	-	COSV52675441,COSV52815950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	307	-	-	-	-	COSV52675441,COSV52815950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	307	-	-	-	-	COSV52675441,COSV52815950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	561	308	103	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	615	308	103	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	558	308	103	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1069225	17:7675186-7675187	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	568	308	103	P/X	cCt/ct	COSV52675441,COSV52815950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	564-565	422-423	141	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	422-423	422-423	141	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	422-423	422-423	141	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	555-556	422-423	141	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	558-559	422-423	141	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	555-556	422-423	141	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52708795,COSV53195443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=39;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	304-305	26-27	9	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	304-305	26-27	9	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	678-679	-	-	-	-	COSV52708795,COSV53195443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	560-561	422-423	141	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	158-159	26-27	9	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	304-305	26-27	9	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	222-223	143-144	48	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52708795,COSV53195443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=70;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52708795,COSV53195443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1602;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	540-541	401-402	134	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	672-673	305-306	102	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	555-556	305-306	102	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	304-305	-	-	-	-	COSV52708795,COSV53195443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	304-305	-	-	-	-	COSV52708795,COSV53195443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	304-305	-	-	-	-	COSV52708795,COSV53195443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	558-559	305-306	102	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	612-613	305-306	102	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	555-556	305-306	102	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
844977	17:7675189-7675189	C	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	565-566	305-306	102	C/WX	tgc/tgGc	COSV52708795,COSV53195443	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	563	421	141	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	421	421	141	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	421	421	141	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	554	421	141	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	557	421	141	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	554	421	141	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=38;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	303	25	9	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	303	25	9	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	677	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	559	421	141	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	157	25	9	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	303	25	9	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	221	142	48	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=72;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1604;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	539	400	134	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	671	304	102	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	554	304	102	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	303	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	303	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	303	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	557	304	102	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	611	304	102	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	554	304	102	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376566	17:7675191-7675191	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	564	304	102	C/G	Tgc/Ggc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	563	421	141	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	421	421	141	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	421	421	141	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	554	421	141	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	557	421	141	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	554	421	141	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=38;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	303	25	9	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	303	25	9	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	677	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	559	421	141	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	157	25	9	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	303	25	9	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	221	142	48	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=72;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1604;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	539	400	134	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	671	304	102	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	554	304	102	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	303	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	303	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	303	-	-	-	-	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	557	304	102	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	611	304	102	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	554	304	102	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376567	17:7675191-7675191	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	564	304	102	C/S	Tgc/Agc	rs1057519978,COSV52675559,COSV52751154,COSV52796306,COSV53037181	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	562-563	420-421	140-141	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	420-421	420-421	140-141	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	420-421	420-421	140-141	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	553-554	420-421	140-141	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	556-557	420-421	140-141	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	553-554	420-421	140-141	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526250	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=37;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	302-303	24-25	8-9	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	302-303	24-25	8-9	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	676-677	-	-	-	-	rs1555526250	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	558-559	420-421	140-141	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	156-157	24-25	8-9	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	302-303	24-25	8-9	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	220-221	141-142	47-48	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526250	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=72;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526250	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1604;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	538-539	399-400	133-134	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	670-671	303-304	101-102	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	553-554	303-304	101-102	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	302-303	-	-	-	-	rs1555526250	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	302-303	-	-	-	-	rs1555526250	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	302-303	-	-	-	-	rs1555526250	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	556-557	303-304	101-102	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	610-611	303-304	101-102	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	553-554	303-304	101-102	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
430592	17:7675191-7675191	GGTCT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	563-564	303-304	101-102	-/RX	-/AGACC	rs1555526250	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	558	416	139	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	416	416	139	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	416	416	139	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	549	416	139	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	552	416	139	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	549	416	139	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597371266,COSV52987330,COSV53124329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=33;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	298	20	7	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	298	20	7	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	672	-	-	-	-	rs1597371266,COSV52987330,COSV53124329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	554	416	139	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	152	20	7	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	298	20	7	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	216	137	46	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597371266,COSV52987330,COSV53124329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=77;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597371266,COSV52987330,COSV53124329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1609;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	534	395	132	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	666	299	100	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	549	299	100	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	298	-	-	-	-	rs1597371266,COSV52987330,COSV53124329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	298	-	-	-	-	rs1597371266,COSV52987330,COSV53124329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	298	-	-	-	-	rs1597371266,COSV52987330,COSV53124329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	552	299	100	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	606	299	100	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	549	299	100	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
811280	17:7675195-7675196	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	559	299	100	K/X	aAg/ag	rs1597371266,COSV52987330,COSV53124329	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	557	415	139	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	415	415	139	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	415	415	139	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	548	415	139	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	551	415	139	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	548	415	139	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=32;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	297	19	7	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	297	19	7	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	671	-	-	-	-	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	553	415	139	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	151	19	7	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	297	19	7	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	215	136	46	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=78;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1610;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	533	394	132	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	665	298	100	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	548	298	100	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	297	-	-	-	-	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	297	-	-	-	-	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	297	-	-	-	-	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	551	298	100	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	605	298	100	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	548	298	100	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634669	17:7675197-7675197	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	558	298	100	K/*	Aag/Tag	rs1212996409,COSV52698907,COSV52754015,COSV53086342,COSV53313307	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	536-551	394-409	132-137	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	394-409	394-409	132-137	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	394-409	394-409	132-137	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	527-542	394-409	132-137	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	530-545	394-409	132-137	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	527-542	394-409	132-137	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203589	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=11;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000504290.5	Transcript	start_lost,5_prime_UTR_variant	276-291	?-13	?-5	-	-	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000504937.5	Transcript	start_lost,5_prime_UTR_variant	276-291	?-13	?-5	-	-	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	650-665	-	-	-	-	rs786203589	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	532-547	394-409	132-137	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000509690.5	Transcript	start_lost,5_prime_UTR_variant	130-145	?-13	?-5	-	-	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000510385.5	Transcript	start_lost,5_prime_UTR_variant	276-291	?-13	?-5	-	-	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	194-209	115-130	39-44	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203589	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=84;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203589	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1616;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-527	?-388	?-130	-	-	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	644-659	277-292	93-98	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	527-542	277-292	93-98	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	276-291	-	-	-	-	rs786203589	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	276-291	-	-	-	-	rs786203589	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	276-291	-	-	-	-	rs786203589	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	530-545	277-292	93-98	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	584-599	277-292	93-98	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	527-542	277-292	93-98	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
187254	17:7675202-7675218	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	537-552	277-292	93-98	KMFCQL/X	AAGATGTTTTGCCAACtg/tg	rs786203589	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	548	406	136	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	406	406	136	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	406	406	136	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	539	406	136	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	542	406	136	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	539	406	136	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=23;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	288	10	4	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000504937.5	Transcript	stop_gained	288	10	4	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	662	-	-	-	-	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	544	406	136	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000509690.5	Transcript	stop_gained	142	10	4	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000510385.5	Transcript	stop_gained	288	10	4	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained	206	127	43	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=87;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1619;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	524	385	129	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	656	289	97	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	539	289	97	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	288	-	-	-	-	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	288	-	-	-	-	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	288	-	-	-	-	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	542	289	97	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	596	289	97	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	539	289	97	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802458	17:7675206-7675206	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	549	289	97	Q/*	Caa/Taa	CM971503,COSV52676850,COSV52715987,COSV52740951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	545-547	403-405	135	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	403-405	403-405	135	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	403-405	403-405	135	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	536-538	403-405	135	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	539-541	403-405	135	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	536-538	403-405	135	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691036	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=20;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	285-287	7-9	3	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	285-287	7-9	3	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	659-661	-	-	-	-	rs1131691036	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	541-543	403-405	135	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	139-141	7-9	3	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	285-287	7-9	3	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	203-205	124-126	42	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691036	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=88;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691036	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1620;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	521-523	382-384	128	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	653-655	286-288	96	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	536-538	286-288	96	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	285-287	-	-	-	-	rs1131691036	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	285-287	-	-	-	-	rs1131691036	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	285-287	-	-	-	-	rs1131691036	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	539-541	286-288	96	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	593-595	286-288	96	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	536-538	286-288	96	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428901	17:7675207-7675209	CC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	546-548	286-288	96	C/X	TGC/GG	rs1131691036	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	545	403	135	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	403	403	135	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	403	403	135	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	536	403	135	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	539	403	135	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	536	403	135	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=20;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	285	7	3	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	285	7	3	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	659	-	-	-	-	COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	541	403	135	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	139	7	3	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	285	7	3	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	203	124	42	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=90;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1622;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	521	382	128	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	653	286	96	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	536	286	96	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	285	-	-	-	-	COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	285	-	-	-	-	COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	285	-	-	-	-	COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	539	286	96	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	593	286	96	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	536	286	96	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1069265	17:7675208-7675209	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	546	286	96	C/X	Tgc/gc	COSV52674321,COSV52706302,COSV52827707	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	545	403	135	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	403	403	135	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	403	403	135	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	536	403	135	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	539	403	135	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	536	403	135	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=20;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	285	7	3	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	285	7	3	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	659	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	541	403	135	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	139	7	3	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	285	7	3	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	203	124	42	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=90;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1622;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	521	382	128	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	653	286	96	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	536	286	96	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	285	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	285	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	285	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	539	286	96	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	593	286	96	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	536	286	96	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376560	17:7675209-7675209	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	546	286	96	C/R	Tgc/Cgc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	545	403	135	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	403	403	135	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	403	403	135	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	536	403	135	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	539	403	135	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	536	403	135	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=20;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	285	7	3	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	285	7	3	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	659	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	541	403	135	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	139	7	3	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	285	7	3	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	203	124	42	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=90;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1622;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	521	382	128	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	653	286	96	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	536	286	96	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	285	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	285	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	285	-	-	-	-	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	539	286	96	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	593	286	96	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	536	286	96	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376563	17:7675209-7675209	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	546	286	96	C/G	Tgc/Ggc	rs1057519975,COSV52674321,COSV52706302,COSV52827707	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	542-543	400-401	134	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	400-401	400-401	134	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	400-401	400-401	134	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	533-534	400-401	134	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	536-537	400-401	134	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	533-534	400-401	134	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=17;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant	282-283	4-5	2	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant	282-283	4-5	2	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	656-657	-	-	-	-	rs1555526286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	538-539	400-401	134	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant	136-137	4-5	2	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant	282-283	4-5	2	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	200-201	121-122	41	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=92;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1624;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	518-519	379-380	127	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	650-651	283-284	95	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	533-534	283-284	95	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	282-283	-	-	-	-	rs1555526286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	282-283	-	-	-	-	rs1555526286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	282-283	-	-	-	-	rs1555526286	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	536-537	283-284	95	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	590-591	283-284	95	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	533-534	283-284	95	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492751	17:7675211-7675211	C	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	543-544	283-284	95	F/CX	ttt/tGtt	rs1555526286	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	542	400	134	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	400	400	134	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	400	400	134	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	533	400	134	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	536	400	134	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	533	400	134	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=17;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	282	4	2	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	282	4	2	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	656	-	-	-	-	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	538	400	134	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	136	4	2	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	282	4	2	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	200	121	41	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=93;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1625;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	518	379	127	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	650	283	95	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	533	283	95	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	282	-	-	-	-	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	282	-	-	-	-	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	282	-	-	-	-	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	536	283	95	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	590	283	95	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	533	283	95	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480953	17:7675212-7675212	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	543	283	95	F/I	Ttt/Att	rs267605077,COSV52660909,COSV52676112,COSV52697695,COSV52923862	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	540-541	398-399	133	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	398-399	398-399	133	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	398-399	398-399	133	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	531-532	398-399	133	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	534-535	398-399	133	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	531-532	398-399	133	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=15;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant,start_lost,start_retained_variant	280-281	2-3	1	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant,start_lost,start_retained_variant	280-281	2-3	1	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	654-655	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	536-537	398-399	133	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant,start_lost,start_retained_variant	134-135	2-3	1	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant,start_lost,start_retained_variant	280-281	2-3	1	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	198-199	119-120	40	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=94;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1626;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant,splice_region_variant	516-517	377-378	126	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	648-649	281-282	94	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	531-532	281-282	94	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	280-281	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	280-281	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	280-281	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	534-535	281-282	94	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	588-589	281-282	94	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	531-532	281-282	94	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1683513	17:7675213-7675213	ATCTTGT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	541-542	281-282	94	M/IQDX	atg/atACAAGATg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	540-541	398-399	133	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	398-399	398-399	133	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	398-399	398-399	133	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	531-532	398-399	133	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	534-535	398-399	133	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	531-532	398-399	133	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597371512	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=15;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant,start_lost	280-281	2-3	1	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000504937.5	Transcript	frameshift_variant,start_lost	280-281	2-3	1	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	654-655	-	-	-	-	rs1597371512	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	536-537	398-399	133	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000509690.5	Transcript	frameshift_variant,start_lost	134-135	2-3	1	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000510385.5	Transcript	frameshift_variant,start_lost	280-281	2-3	1	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	198-199	119-120	40	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597371512	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=94;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597371512	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1626;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant,splice_region_variant	516-517	377-378	126	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	648-649	281-282	94	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	531-532	281-282	94	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	280-281	-	-	-	-	rs1597371512	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	280-281	-	-	-	-	rs1597371512	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	280-281	-	-	-	-	rs1597371512	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	534-535	281-282	94	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	588-589	281-282	94	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	531-532	281-282	94	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
824462	17:7675213-7675213	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	541-542	281-282	94	M/IX	atg/atTg	rs1597371512	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	538	396	132	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	396	396	132	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	396	396	132	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	529	396	132	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	532	396	132	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	529	396	132	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=13;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	278	-	-	-	-	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	278	-	-	-	-	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	652	-	-	-	-	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	534	396	132	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	132	-	-	-	-	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	278	-	-	-	-	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	196	117	39	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=97;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1629;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	646	279	93	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	529	279	93	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	278	-	-	-	-	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	278	-	-	-	-	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	278	-	-	-	-	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	532	279	93	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	586	279	93	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	529	279	93	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376624	17:7675216-7675216	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	539	279	93	K/N	aaG/aaC	rs866775781,COSV52688381,COSV52705927,COSV52891203,COSV53339296	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	537	395	132	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	395	395	132	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	395	395	132	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	528	395	132	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	531	395	132	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	528	395	132	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=12;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	277	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	277	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	651	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	533	395	132	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	131	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	277	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	195	116	39	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=98;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1630;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	645	278	93	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	528	278	93	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	277	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	277	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	277	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	531	278	93	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	585	278	93	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	528	278	93	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376625	17:7675217-7675217	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	538	278	93	K/R	aAg/aGg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	537	395	132	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	395	395	132	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	395	395	132	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	528	395	132	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	531	395	132	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	528	395	132	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=12;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	277	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	277	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	651	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	533	395	132	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	131	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	277	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	195	116	39	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=98;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1630;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	645	278	93	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	528	278	93	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	277	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	277	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	277	-	-	-	-	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	531	278	93	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	585	278	93	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	528	278	93	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376627	17:7675217-7675217	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	538	278	93	K/T	aAg/aCg	rs1057519996,COSV52666637,COSV52701687,COSV52759171	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	536	394	132	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	394	394	132	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	394	394	132	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	527	394	132	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	530	394	132	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	527	394	132	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=11;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	276	-	-	-	-	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	276	-	-	-	-	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	650	-	-	-	-	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	532	394	132	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	130	-	-	-	-	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	276	-	-	-	-	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	194	115	39	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=99;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1631;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	644	277	93	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	527	277	93	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	276	-	-	-	-	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	276	-	-	-	-	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	276	-	-	-	-	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	530	277	93	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	584	277	93	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	527	277	93	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376626	17:7675218-7675218	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	537	277	93	K/E	Aag/Gag	rs747342068,CM086989,CM973641,COSV52689323,COSV52708494,COSV52979406,COSV53353999	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,uncertain_significance,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	535	393	131	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	393	393	131	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	393	393	131	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	526	393	131	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	529	393	131	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	526	393	131	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=10;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	275	-	-	-	-	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	275	-	-	-	-	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	649	-	-	-	-	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	531	393	131	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	129	-	-	-	-	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	275	-	-	-	-	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	193	114	38	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=100;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1632;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	643	276	92	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	526	276	92	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	275	-	-	-	-	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	275	-	-	-	-	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	275	-	-	-	-	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	529	276	92	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	583	276	92	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	526	276	92	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634698	17:7675218-7675219	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	536	276	92	N/X	aaC/aa	rs1567554408,COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-536	?-394	?-132	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-394	?-394	?-132	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-394	?-394	?-132	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-527	?-394	?-132	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-530	?-394	?-132	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-527	?-394	?-132	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	188-276	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	188-276	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,non_coding_transcript_exon_variant,intron_variant	?-650	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-532	?-394	?-132	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,5_prime_UTR_variant,intron_variant	?-130	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	188-276	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-194	?-115	?-39	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=99;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1631;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-644	?-277	?-93	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-527	?-277	?-93	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	188-276	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	188-276	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	188-276	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-530	?-277	?-93	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-584	?-277	?-93	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-527	?-277	?-93	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
944769	17:7675218-7675306	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant,NMD_transcript_variant	?-537	?-277	?-93	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	534	392	131	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	392	392	131	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	392	392	131	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	525	392	131	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	528	392	131	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	525	392	131	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=9;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	274	-	-	-	-	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	274	-	-	-	-	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	648	-	-	-	-	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	530	392	131	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	128	-	-	-	-	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	274	-	-	-	-	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	192	113	38	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=101;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1633;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	642	275	92	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	525	275	92	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	274	-	-	-	-	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	274	-	-	-	-	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	274	-	-	-	-	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	528	275	92	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	582	275	92	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	525	275	92	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
428902	17:7675220-7675220	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	535	275	92	N/I	aAc/aTc	rs1131691037,CM087281,CM159290,COSV52670715,COSV52718021,COSV53252418	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	532	390	130	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	390	390	130	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	390	390	130	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	523	390	130	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	526	390	130	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	523	390	130	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=7;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	272	-	-	-	-	COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	272	-	-	-	-	COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	646	-	-	-	-	COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	528	390	130	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	126	-	-	-	-	COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	272	-	-	-	-	COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	190	111	37	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=103;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1635;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	640	273	91	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	523	273	91	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	272	-	-	-	-	COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	272	-	-	-	-	COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	272	-	-	-	-	COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	526	273	91	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	580	273	91	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	523	273	91	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1458610	17:7675221-7675222	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	533	273	91	L/X	ctC/ct	COSV52782624	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	530	388	130	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	388	388	130	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	388	388	130	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	521	388	130	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	524	388	130	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	521	388	130	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	270	-	-	-	-	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	270	-	-	-	-	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	644	-	-	-	-	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	526	388	130	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	124	-	-	-	-	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	270	-	-	-	-	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	188	109	37	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=105;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1637;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	638	271	91	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	521	271	91	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	270	-	-	-	-	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	270	-	-	-	-	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	270	-	-	-	-	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	524	271	91	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	578	271	91	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	521	271	91	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1366432	17:7675223-7675224	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	531	271	91	L/X	Ctc/tc	CM016206,COSV52686543,COSV52692226,COSV99368721	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	531	389	130	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	389	389	130	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	389	389	130	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	522	389	130	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	525	389	130	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	522	389	130	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	645	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	527	389	130	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	125	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	189	110	37	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=104;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1636;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	639	272	91	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	522	272	91	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	525	272	91	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	579	272	91	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	522	272	91	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
428873	17:7675223-7675223	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	532	272	91	L/P	cTc/cCc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	531	389	130	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	389	389	130	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	389	389	130	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	522	389	130	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	525	389	130	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	522	389	130	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	645	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	527	389	130	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	125	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	189	110	37	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=104;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1636;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,splice_region_variant,intron_variant	-	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	639	272	91	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	522	272	91	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	525	272	91	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	579	272	91	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	522	272	91	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
824351	17:7675223-7675223	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	532	272	91	L/H	cTc/cAc	rs1131691013,CM120849,CM134998,COSV52681833,COSV52696302,COSV52721346,COSV53165479	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	525	383	128	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	383	383	128	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	383	383	128	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	516	383	128	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	519	383	128	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	516	383	128	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000503591.1	Transcript	incomplete_terminal_codon_variant,coding_sequence_variant	565	383	128	X	cC/c	rs1597371666,COSV53283607	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	265	-	-	-	-	rs1597371666,COSV53283607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	265	-	-	-	-	rs1597371666,COSV53283607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	639	-	-	-	-	rs1597371666,COSV53283607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	521	383	128	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	119	-	-	-	-	rs1597371666,COSV53283607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	265	-	-	-	-	rs1597371666,COSV53283607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	183	104	35	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597371666,COSV53283607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=110;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597371666,COSV53283607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1642;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597371666,COSV53283607	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	633	266	89	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	516	266	89	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	265	-	-	-	-	rs1597371666,COSV53283607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	265	-	-	-	-	rs1597371666,COSV53283607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	265	-	-	-	-	rs1597371666,COSV53283607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	519	266	89	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	573	266	89	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	516	266	89	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
659670	17:7675228-7675229	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	526	266	89	P/X	cCt/ct	rs1597371666,COSV53283607	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	522	380	127	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	380	380	127	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	380	380	127	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	513	380	127	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	516	380	127	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	513	380	127	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	562	380	127	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	262	-	-	-	-	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	262	-	-	-	-	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	636	-	-	-	-	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	518	380	127	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	116	-	-	-	-	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	262	-	-	-	-	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	180	101	34	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=113;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1645;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	630	263	88	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	513	263	88	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	262	-	-	-	-	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	262	-	-	-	-	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	262	-	-	-	-	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	516	263	88	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	570	263	88	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	513	263	88	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
656751	17:7675232-7675232	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	523	263	88	S/Y	tCc/tAc	rs730881999,COSV52666031,COSV52675881,COSV52731113,COSV52828604	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	521	379	127	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	379	379	127	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	379	379	127	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	512	379	127	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	515	379	127	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	512	379	127	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	561	379	127	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	261	-	-	-	-	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	261	-	-	-	-	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	635	-	-	-	-	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	517	379	127	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	115	-	-	-	-	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	261	-	-	-	-	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	179	100	34	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=114;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1646;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	629	262	88	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	512	262	88	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	261	-	-	-	-	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	261	-	-	-	-	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	261	-	-	-	-	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	515	262	88	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	569	262	88	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	512	262	88	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
934410	17:7675233-7675233	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	522	262	88	S/P	Tcc/Ccc	COSV52667433,COSV52678360,COSV52751962	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-519	?-377	?-126	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-377	?-377	?-126	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-377	?-377	?-126	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-510	?-377	?-126	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-513	?-377	?-126	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-510	?-377	?-126	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-559	?-377	?-126	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	247-259	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	247-259	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,non_coding_transcript_exon_variant,intron_variant	?-633	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-515	?-377	?-126	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,5_prime_UTR_variant,intron_variant	?-113	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	247-259	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-177	?-98	?-33	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=116;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1648;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-627	?-260	?-87	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-510	?-260	?-87	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	247-259	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	247-259	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	247-259	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-513	?-260	?-87	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-567	?-260	?-87	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-510	?-260	?-87	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1333732	17:7675234-7675247	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant,NMD_transcript_variant	?-520	?-260	?-87	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained,splice_region_variant	520	378	126	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained,splice_region_variant	378	378	126	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained,splice_region_variant	378	378	126	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained,splice_region_variant	511	378	126	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained,splice_region_variant	514	378	126	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained,splice_region_variant	511	378	126	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained,splice_region_variant	560	378	126	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	260	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	260	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	634	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained,splice_region_variant	516	378	126	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,5_prime_UTR_variant	114	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	260	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained,splice_region_variant	178	99	33	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=115;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1647;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained,splice_region_variant	628	261	87	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained,splice_region_variant	511	261	87	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	260	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	260	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	260	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained,splice_region_variant	514	261	87	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained,splice_region_variant	568	261	87	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained,splice_region_variant	511	261	87	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1453627	17:7675234-7675234	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,splice_region_variant,NMD_transcript_variant	521	261	87	Y/*	taC/taA	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained,frameshift_variant,splice_region_variant	519-520	377-378	126	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained,frameshift_variant,splice_region_variant	377-378	377-378	126	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained,frameshift_variant,splice_region_variant	377-378	377-378	126	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained,frameshift_variant,splice_region_variant	510-511	377-378	126	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained,frameshift_variant,splice_region_variant	513-514	377-378	126	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained,frameshift_variant,splice_region_variant	510-511	377-378	126	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained,frameshift_variant,splice_region_variant	559-560	377-378	126	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	259-260	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	259-260	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	633-634	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained,frameshift_variant,splice_region_variant	515-516	377-378	126	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,5_prime_UTR_variant	113-114	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	259-260	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained,frameshift_variant,splice_region_variant	177-178	98-99	33	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=115;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1647;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained,frameshift_variant,splice_region_variant	627-628	260-261	87	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained,frameshift_variant,splice_region_variant	510-511	260-261	87	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	259-260	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	259-260	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	259-260	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained,frameshift_variant,splice_region_variant	513-514	260-261	87	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained,frameshift_variant,splice_region_variant	567-568	260-261	87	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained,frameshift_variant,splice_region_variant	510-511	260-261	87	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1734681	17:7675234-7675234	TACT	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,frameshift_variant,splice_region_variant,NMD_transcript_variant	520-521	260-261	87	Y/*VX	tac/taAGTAc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained,splice_region_variant	520	378	126	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained,splice_region_variant	378	378	126	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained,splice_region_variant	378	378	126	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained,splice_region_variant	511	378	126	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained,splice_region_variant	514	378	126	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained,splice_region_variant	511	378	126	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained,splice_region_variant	560	378	126	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	260	-	-	-	-	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	260	-	-	-	-	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	634	-	-	-	-	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained,splice_region_variant	516	378	126	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,5_prime_UTR_variant	114	-	-	-	-	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	260	-	-	-	-	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000514944.5	Transcript	stop_gained,splice_region_variant	178	99	33	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=115;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1647;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained,splice_region_variant	628	261	87	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained,splice_region_variant	511	261	87	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	260	-	-	-	-	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	260	-	-	-	-	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	260	-	-	-	-	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained,splice_region_variant	514	261	87	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained,splice_region_variant	568	261	87	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained,splice_region_variant	511	261	87	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
578988	17:7675234-7675234	C	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,splice_region_variant,NMD_transcript_variant	521	261	87	Y/*	taC/taG	rs1567554500,CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant,splice_region_variant	518	376	126	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant,splice_region_variant	376	376	126	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant,splice_region_variant	376	376	126	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant,splice_region_variant	509	376	126	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant,splice_region_variant	512	376	126	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant,splice_region_variant	509	376	126	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant,splice_region_variant	558	376	126	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	258	-	-	-	-	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	258	-	-	-	-	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	632	-	-	-	-	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant,splice_region_variant	514	376	126	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,5_prime_UTR_variant	112	-	-	-	-	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	258	-	-	-	-	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant,splice_region_variant	176	97	33	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=117;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1649;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant,splice_region_variant	626	259	87	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant,splice_region_variant	509	259	87	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	258	-	-	-	-	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	258	-	-	-	-	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	258	-	-	-	-	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant,splice_region_variant	512	259	87	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant,splice_region_variant	566	259	87	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant,splice_region_variant	509	259	87	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
634700	17:7675235-7675236	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,splice_region_variant,NMD_transcript_variant	519	259	87	Y/X	Tac/ac	rs1567554542,CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant,splice_region_variant	518	376	126	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant,splice_region_variant	376	376	126	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant,splice_region_variant	376	376	126	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant,splice_region_variant	509	376	126	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant,splice_region_variant	512	376	126	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant,splice_region_variant	509	376	126	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant,splice_region_variant	558	376	126	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	258	-	-	-	-	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	258	-	-	-	-	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	632	-	-	-	-	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant,splice_region_variant	514	376	126	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,5_prime_UTR_variant	112	-	-	-	-	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	258	-	-	-	-	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant,splice_region_variant	176	97	33	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=117;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1649;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant,splice_region_variant	626	259	87	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant,splice_region_variant	509	259	87	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	258	-	-	-	-	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	258	-	-	-	-	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	258	-	-	-	-	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant,splice_region_variant	512	259	87	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant,splice_region_variant	566	259	87	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant,splice_region_variant	509	259	87	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1734755	17:7675236-7675236	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,splice_region_variant,NMD_transcript_variant	519	259	87	Y/H	Tac/Cac	CM118879,COSV52661802,COSV52809424,COSV53031989,COSV53515469	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	257	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	257	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	257	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=118;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1650;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	257	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	257	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	257	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1210292	17:7675237-7675237	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	257	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	257	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	257	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=118;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1650;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	257	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	257	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	257	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
481003	17:7675237-7675237	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs868137297,CS1313555,COSV52688618,COSV52749979,COSV52994579,COSV52996344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	256	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	256	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	256	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=119;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1651;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	256	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	256	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	256	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
186236	17:7675238-7675238	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	256	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	256	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	256	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=119;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1651;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	256	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	256	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	256	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
458540	17:7675238-7675238	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs786202799,CS114003,COSV52689235,COSV52691326,COSV53121815,COSV53758902	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	425-?	283-?	95-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	283-?	283-?	95-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	283-?	283-?	95-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	416-?	283-?	95-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	419-?	283-?	95-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	416-?	283-?	95-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	465-?	283-?	95-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526462	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=480;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526462	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=480;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,non_coding_transcript_exon_variant,intron_variant	539-?	-	-	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	421-?	283-?	95-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526462	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526462	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=480;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526462	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526462	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=854;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526462	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2386;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	422-?	283-?	95-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	533-?	166-?	56-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	416-?	166-?	56-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526462	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=480;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526462	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=480;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526462	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=480;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	419-?	166-?	56-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	473-?	166-?	56-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant	416-?	166-?	56-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
406569	17:7675972-7676086	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,coding_sequence_variant,intron_variant,NMD_transcript_variant	426-?	166-?	56-?	-	-	rs1555526462	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=486;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=486;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=486;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=860;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2392;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=486;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=486;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=486;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075308	17:7675978-7675992	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,splice_donor_5th_base_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_5th_base_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=870;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2402;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_5th_base_variant,intron_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634777	17:7675989-7675989	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_5th_base_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526466,COSV52944494,COSV53057829,COSV53328358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=873;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2405;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
439316	17:7675992-7675992	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=873;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2405;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482210	17:7675992-7675992	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=873;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2405;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528256	17:7675992-7675992	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526469,CS147127,COSV52663814,COSV52664353,COSV52730362	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=873;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2405;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=499;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
528263	17:7675992-7675992	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526470,COSV53061158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=874;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2406;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634702	17:7675993-7675993	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=874;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2406;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
635393	17:7675993-7675993	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=874;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2406;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
664392	17:7675993-7675993	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1567555445,CS951538,COSV52663569,COSV52668477,COSV52702628	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	517	375	125	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,synonymous_variant	375	375	125	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,synonymous_variant	375	375	125	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,synonymous_variant	508	375	125	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	511	375	125	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,synonymous_variant	508	375	125	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,synonymous_variant	557	375	125	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	631	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,synonymous_variant	513	375	125	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=875;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2407;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,synonymous_variant	514	375	125	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,synonymous_variant	625	258	86	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,synonymous_variant	508	258	86	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,synonymous_variant	511	258	86	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,synonymous_variant	565	258	86	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,synonymous_variant	508	258	86	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
177825	17:7675994-7675994	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,synonymous_variant,NMD_transcript_variant	518	258	86	T	acG/acA	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	517	375	125	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,synonymous_variant	375	375	125	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,synonymous_variant	375	375	125	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,synonymous_variant	508	375	125	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	511	375	125	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,synonymous_variant	508	375	125	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,synonymous_variant	557	375	125	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	631	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,synonymous_variant	513	375	125	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=875;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2407;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,synonymous_variant	514	375	125	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,synonymous_variant	625	258	86	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,synonymous_variant	508	258	86	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,synonymous_variant	511	258	86	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,synonymous_variant	565	258	86	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,synonymous_variant	508	258	86	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
237948	17:7675994-7675994	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,synonymous_variant,NMD_transcript_variant	518	258	86	T	acG/acT	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	517	375	125	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,synonymous_variant	375	375	125	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,synonymous_variant	375	375	125	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,synonymous_variant	508	375	125	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	511	375	125	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,synonymous_variant	508	375	125	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,synonymous_variant	557	375	125	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	631	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,synonymous_variant	513	375	125	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=875;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2407;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,synonymous_variant	514	375	125	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,synonymous_variant	625	258	86	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,synonymous_variant	508	258	86	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,synonymous_variant	511	258	86	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,synonymous_variant	565	258	86	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,synonymous_variant	508	258	86	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
480746	17:7675994-7675994	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,synonymous_variant,NMD_transcript_variant	518	258	86	T	acG/acC	rs55863639,CS004351,CS011573,CS971913,COSV52665709,COSV52718605,COSV52726641,COSV53120615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant,splice_region_variant	516	374	125	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant,splice_region_variant	374	374	125	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant,splice_region_variant	374	374	125	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant,splice_region_variant	507	374	125	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant,splice_region_variant	510	374	125	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant,splice_region_variant	507	374	125	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant,splice_region_variant	556	374	125	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	630	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant,splice_region_variant	512	374	125	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=876;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2408;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant,splice_region_variant	513	374	125	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant,splice_region_variant	624	257	86	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant,splice_region_variant	507	257	86	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant,splice_region_variant	510	257	86	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant,splice_region_variant	564	257	86	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant,splice_region_variant	507	257	86	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
376667	17:7675995-7675995	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,splice_region_variant,NMD_transcript_variant	517	257	86	T/R	aCg/aGg	rs786201057,CM102351,CM157948,COSV52667346,COSV52673504,COSV52688693,COSV99037266	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant,splice_region_variant	515-516	373-374	125	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant,splice_region_variant	373-374	373-374	125	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant,splice_region_variant	373-374	373-374	125	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant,splice_region_variant	506-507	373-374	125	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant,splice_region_variant	509-510	373-374	125	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant,splice_region_variant	506-507	373-374	125	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant,splice_region_variant	555-556	373-374	125	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	629-630	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant,splice_region_variant	511-512	373-374	125	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=876;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2408;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant,splice_region_variant	512-513	373-374	125	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant,splice_region_variant	623-624	256-257	86	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant,splice_region_variant	506-507	256-257	86	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant,splice_region_variant	509-510	256-257	86	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant,splice_region_variant	563-564	256-257	86	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant,splice_region_variant	506-507	256-257	86	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
851884	17:7675995-7675995	TGCAAGTCACAGT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,splice_region_variant,NMD_transcript_variant	516-517	256-257	86	T/NCDLHX	acg/aACTGTGACTTGCAcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	514	372	124	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	372	372	124	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	372	372	124	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	505	372	124	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	508	372	124	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	505	372	124	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	554	372	124	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	628	-	-	-	-	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	510	372	124	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=878;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2410;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	511	372	124	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	622	255	85	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	505	255	85	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	508	255	85	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	562	255	85	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	505	255	85	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458537	17:7675997-7675997	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	515	255	85	C/*	tgC/tgA	rs1555526478,CM1210346,COSV52731101,COSV52944837	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	513-514	371-372	124	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	371-372	371-372	124	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	371-372	371-372	124	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	504-505	371-372	124	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	507-508	371-372	124	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	504-505	371-372	124	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	553-554	371-372	124	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1267047192,COSV53205177	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1267047192,COSV53205177	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	627-628	-	-	-	-	rs1267047192,COSV53205177	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	509-510	371-372	124	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1267047192,COSV53205177	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1267047192,COSV53205177	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1267047192,COSV53205177	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1267047192,COSV53205177	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=878;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1267047192,COSV53205177	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2410;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	510-511	371-372	124	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	621-622	254-255	85	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	504-505	254-255	85	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1267047192,COSV53205177	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1267047192,COSV53205177	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1267047192,COSV53205177	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	507-508	254-255	85	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	561-562	254-255	85	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	504-505	254-255	85	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634664	17:7675997-7675997	C	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	514-515	254-255	85	C/WX	tgc/tgGc	rs1267047192,COSV53205177	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	503-513	361-371	121-124	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	361-371	361-371	121-124	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	361-371	361-371	121-124	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	494-504	361-371	121-124	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	497-507	361-371	121-124	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	494-504	361-371	121-124	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	543-553	361-371	121-124	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555504	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=505;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555504	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=505;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	617-627	-	-	-	-	rs1567555504	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	499-509	361-371	121-124	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567555504	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555504	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=505;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567555504	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555504	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=879;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555504	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2411;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	500-510	361-371	121-124	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	611-621	244-254	82-85	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	494-504	244-254	82-85	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555504	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=505;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555504	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=505;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555504	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=505;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	497-507	244-254	82-85	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	551-561	244-254	82-85	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	494-504	244-254	82-85	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634671	17:7675997-7676008	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	504-514	244-254	82-85	SVTC/X	TCTGTGACTTGc/c	rs1567555504	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	507-508	365-366	122	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	365-366	365-366	122	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	365-366	365-366	122	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	498-499	365-366	122	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	501-502	365-366	122	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	498-499	365-366	122	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	547-548	365-366	122	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	621-622	-	-	-	-	rs587780067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	503-504	365-366	122	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587780067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587780067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=884;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2416;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	504-505	365-366	122	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	615-616	248-249	83	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	498-499	248-249	83	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780067	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	501-502	248-249	83	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	555-556	248-249	83	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	498-499	248-249	83	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
127809	17:7676002-7676004	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	508-509	248-249	83	V/X	gTG/g	rs587780067	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	507-508	365-366	122	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	365-366	365-366	122	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	365-366	365-366	122	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	498-499	365-366	122	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	501-502	365-366	122	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	498-499	365-366	122	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	547-548	365-366	122	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373467,COSV52807421,COSV53155976	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373467,COSV52807421,COSV53155976	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	621-622	-	-	-	-	rs1597373467,COSV52807421,COSV53155976	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	503-504	365-366	122	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597373467,COSV52807421,COSV53155976	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373467,COSV52807421,COSV53155976	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597373467,COSV52807421,COSV53155976	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373467,COSV52807421,COSV53155976	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=884;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373467,COSV52807421,COSV53155976	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2416;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	504-505	365-366	122	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	615-616	248-249	83	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	498-499	248-249	83	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373467,COSV52807421,COSV53155976	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373467,COSV52807421,COSV53155976	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373467,COSV52807421,COSV53155976	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	501-502	248-249	83	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	555-556	248-249	83	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	498-499	248-249	83	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
817074	17:7676003-7676003	ACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAG	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	508-509	248-249	83	V/VWASCILGQPSLX	gtg/gtCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTg	rs1597373467,COSV52807421,COSV53155976	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	506-507	364-365	122	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	364-365	364-365	122	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	364-365	364-365	122	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	497-498	364-365	122	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	500-501	364-365	122	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	497-498	364-365	122	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	546-547	364-365	122	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526495,COSV52898742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=511;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526495,COSV52898742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=511;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	620-621	-	-	-	-	rs1555526495,COSV52898742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	502-503	364-365	122	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526495,COSV52898742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526495,COSV52898742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=511;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526495,COSV52898742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526495,COSV52898742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=885;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526495,COSV52898742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2417;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	503-504	364-365	122	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	614-615	247-248	83	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	497-498	247-248	83	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526495,COSV52898742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=511;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526495,COSV52898742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=511;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526495,COSV52898742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=511;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	500-501	247-248	83	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	554-555	247-248	83	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	497-498	247-248	83	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
430665	17:7676004-7676004	CAGACTTGGCTGTCCCAGAATGCAAGAAGCC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	507-508	247-248	83	V/GLLAFWDSQVCX	gtg/gGGCTTCTTGCATTCTGGGACAGCCAAGTCTGtg	rs1555526495,COSV52898742	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	500	358	120	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	358	358	120	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	358	358	120	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	491	358	120	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	494	358	120	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	491	358	120	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	540	358	120	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=518;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=518;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	614	-	-	-	-	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	496	358	120	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=518;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2424;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	497	358	120	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	608	241	81	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	491	241	81	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=518;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=518;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=518;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	494	241	81	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	548	241	81	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	491	241	81	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
12363	17:7676011-7676011	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	501	241	81	K/*	Aag/Tag	rs121912658,CM921039,COSV52676498,COSV52692352,COSV53551619,COSV53685479	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	499	357	119	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	357	357	119	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	357	357	119	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	490	357	119	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	493	357	119	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	490	357	119	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	539	357	119	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373517,COSV52702653,COSV52827728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=519;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373517,COSV52702653,COSV52827728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=519;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	613	-	-	-	-	rs1597373517,COSV52702653,COSV52827728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	495	357	119	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597373517,COSV52702653,COSV52827728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373517,COSV52702653,COSV52827728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=519;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597373517,COSV52702653,COSV52827728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373517,COSV52702653,COSV52827728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=893;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373517,COSV52702653,COSV52827728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2425;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	496	357	119	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	607	240	80	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	490	240	80	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373517,COSV52702653,COSV52827728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=519;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373517,COSV52702653,COSV52827728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=519;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373517,COSV52702653,COSV52827728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=519;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	493	240	80	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	547	240	80	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	490	240	80	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
823953	17:7676011-7676012	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	500	240	80	A/X	gcC/gc	rs1597373517,COSV52702653,COSV52827728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	496	354	118	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	354	354	118	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	354	354	118	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	487	354	118	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	490	354	118	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	487	354	118	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	536	354	118	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	610	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	492	354	118	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=896;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2428;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	493	354	118	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	604	237	79	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	487	237	79	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	490	237	79	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	544	237	79	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	487	237	79	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1732574	17:7676014-7676015	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	497	237	79	T/X	acA/ac	COSV53220114	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	487-494	345-352	115-118	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	345-352	345-352	115-118	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	345-352	345-352	115-118	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	478-485	345-352	115-118	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	481-488	345-352	115-118	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	478-485	345-352	115-118	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	527-534	345-352	115-118	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=524;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=524;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	601-608	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	483-490	345-352	115-118	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=524;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=898;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2430;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	484-491	345-352	115-118	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	595-602	228-235	76-79	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	478-485	228-235	76-79	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=524;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=524;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=524;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	481-488	228-235	76-79	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	535-542	228-235	76-79	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	478-485	228-235	76-79	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1731558	17:7676017-7676024	GGCT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	488-495	228-235	76-79	HSGT/QAX	caTTCTGGGAca/caAGCCca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	488-489	346-347	116	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	346-347	346-347	116	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	346-347	346-347	116	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	479-480	346-347	116	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	482-483	346-347	116	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	479-480	346-347	116	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	528-529	346-347	116	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526524	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=529;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526524	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=529;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	602-603	-	-	-	-	rs1555526524	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	484-485	346-347	116	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526524	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526524	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=529;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526524	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526524	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=903;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526524	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2435;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	485-486	346-347	116	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	596-597	229-230	77	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	479-480	229-230	77	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526524	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=529;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526524	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=529;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526524	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=529;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	482-483	229-230	77	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	536-537	229-230	77	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	479-480	229-230	77	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545871	17:7676022-7676022	AATGCAA	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	489-490	229-230	77	S/FAFX	tct/tTTGCATTct	rs1555526524	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	485	343	115	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	343	343	115	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	343	343	115	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	476	343	115	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	479	343	115	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	476	343	115	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	525	343	115	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52889393,COSV52966672	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52889393,COSV52966672	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	599	-	-	-	-	COSV52889393,COSV52966672	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	481	343	115	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52889393,COSV52966672	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52889393,COSV52966672	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52889393,COSV52966672	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52889393,COSV52966672	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=907;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52889393,COSV52966672	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2439;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	482	343	115	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	593	226	76	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	476	226	76	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52889393,COSV52966672	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52889393,COSV52966672	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52889393,COSV52966672	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	479	226	76	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	533	226	76	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	476	226	76	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
920389	17:7676025-7676026	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	486	226	76	H/X	Cat/at	COSV52889393,COSV52966672	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	484-485	342-343	114-115	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	342-343	342-343	114-115	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	342-343	342-343	114-115	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	475-476	342-343	114-115	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	478-479	342-343	114-115	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	475-476	342-343	114-115	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	524-525	342-343	114-115	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373605	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373605	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	598-599	-	-	-	-	rs1597373605	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	480-481	342-343	114-115	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597373605	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373605	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597373605	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373605	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=907;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373605	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2439;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	481-482	342-343	114-115	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	592-593	225-226	75-76	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	475-476	225-226	75-76	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373605	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373605	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373605	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	478-479	225-226	75-76	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	532-533	225-226	75-76	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	475-476	225-226	75-76	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
661054	17:7676026-7676026	C	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	485-486	225-226	75-76	-/X	-/G	rs1597373605	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	483	341	114	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	341	341	114	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	341	341	114	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	474	341	114	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	477	341	114	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	474	341	114	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	523	341	114	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs781724995,CD084237,COSV52753440	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=535;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs781724995,CD084237,COSV52753440	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=535;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	597	-	-	-	-	rs781724995,CD084237,COSV52753440	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	479	341	114	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs781724995,CD084237,COSV52753440	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs781724995,CD084237,COSV52753440	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=535;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs781724995,CD084237,COSV52753440	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs781724995,CD084237,COSV52753440	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=909;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs781724995,CD084237,COSV52753440	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2441;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	480	341	114	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	591	224	75	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	474	224	75	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs781724995,CD084237,COSV52753440	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=535;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs781724995,CD084237,COSV52753440	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=535;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs781724995,CD084237,COSV52753440	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=535;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	477	224	75	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	531	224	75	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	474	224	75	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
634753	17:7676028-7676028	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	484	224	75	L/*	tTg/tAg	rs781724995,CD084237,COSV52753440	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	470-481	328-339	110-113	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	328-339	328-339	110-113	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	328-339	328-339	110-113	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	461-472	328-339	110-113	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	464-475	328-339	110-113	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	461-472	328-339	110-113	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000503591.1	Transcript	inframe_deletion	510-521	328-339	110-113	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782490	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782490	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	584-595	-	-	-	-	rs587782490	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000508793.5	Transcript	inframe_deletion	466-477	328-339	110-113	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587782490	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782490	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587782490	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782490	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=911;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782490	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2443;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000604348.5	Transcript	inframe_deletion	467-478	328-339	110-113	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	578-589	211-222	71-74	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	461-472	211-222	71-74	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782490	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782490	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782490	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	464-475	211-222	71-74	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	518-529	211-222	71-74	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	461-472	211-222	71-74	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
142480	17:7676029-7676041	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	471-482	211-222	71-74	RLGF/-	CGTCTGGGCTTC/-	rs587782490	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	464-481	322-339	108-113	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	322-339	322-339	108-113	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	322-339	322-339	108-113	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	455-472	322-339	108-113	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	458-475	322-339	108-113	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	455-472	322-339	108-113	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000503591.1	Transcript	inframe_deletion	504-521	322-339	108-113	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs886039495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs886039495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	578-595	-	-	-	-	rs886039495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000508793.5	Transcript	inframe_deletion	460-477	322-339	108-113	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs886039495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs886039495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs886039495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs886039495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=911;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs886039495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2443;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000604348.5	Transcript	inframe_deletion	461-478	322-339	108-113	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	572-589	205-222	69-74	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	455-472	205-222	69-74	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs886039495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs886039495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs886039495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	458-475	205-222	69-74	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	512-529	205-222	69-74	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	455-472	205-222	69-74	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
265351	17:7676029-7676047	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	465-482	205-222	69-74	GFRLGF/-	GGTTTCCGTCTGGGCTTC/-	rs886039495	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	469-473	327-331	109-111	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	327-331	327-331	109-111	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	327-331	327-331	109-111	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	460-464	327-331	109-111	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	463-467	327-331	109-111	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	460-464	327-331	109-111	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	509-513	327-331	109-111	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	583-587	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	465-469	327-331	109-111	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=919;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2451;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	466-470	327-331	109-111	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	577-581	210-214	70-72	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	460-464	210-214	70-72	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	463-467	210-214	70-72	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	517-521	210-214	70-72	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	460-464	210-214	70-72	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1074964	17:7676037-7676042	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	470-474	210-214	70-72	FRL/FX	ttCCGTCtg/tttg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	473	331	111	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	331	331	111	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	331	331	111	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	464	331	111	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	467	331	111	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	464	331	111	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	513	331	111	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	587	-	-	-	-	COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	469	331	111	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=919;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2451;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	470	331	111	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	581	214	72	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	464	214	72	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	467	214	72	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	521	214	72	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	464	214	72	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1679814	17:7676037-7676038	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	474	214	72	L/X	Ctg/tg	COSV105032054,COSV53244109	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	474	332	111	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	332	332	111	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	332	332	111	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	465	332	111	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	468	332	111	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	465	332	111	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	514	332	111	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=544;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=544;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	588	-	-	-	-	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	470	332	111	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=544;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=918;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2450;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	471	332	111	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	582	215	72	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	465	215	72	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=544;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=544;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=544;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	468	215	72	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	522	215	72	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	465	215	72	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
376631	17:7676037-7676037	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	475	215	72	L/R	cTg/cGg	rs1057519997,CX942126,COSV52676090,COSV52699193,COSV52985195	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	466-473	324-331	108-111	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	324-331	324-331	108-111	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	324-331	324-331	108-111	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	457-464	324-331	108-111	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	460-467	324-331	108-111	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	457-464	324-331	108-111	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	506-513	324-331	108-111	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52745301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52745301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	580-587	-	-	-	-	COSV52745301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	462-469	324-331	108-111	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52745301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52745301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52745301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52745301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=919;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52745301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2451;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	463-470	324-331	108-111	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	574-581	207-214	69-72	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	457-464	207-214	69-72	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52745301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52745301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52745301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	460-467	207-214	69-72	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	514-521	207-214	69-72	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	457-464	207-214	69-72	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
997929	17:7676038-7676045	TTT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	467-474	207-214	69-72	GFRL/GNX	ggTTTCCGTCtg/ggAAAtg	COSV52745301	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	471-472	329-330	110	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	329-330	329-330	110	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	329-330	329-330	110	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	462-463	329-330	110	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	465-466	329-330	110	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	462-463	329-330	110	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	511-512	329-330	110	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	585-586	-	-	-	-	rs1131691004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	467-468	329-330	110	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1131691004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1131691004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=920;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2452;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	468-469	329-330	110	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	579-580	212-213	71	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	462-463	212-213	71	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691004	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	465-466	212-213	71	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	519-520	212-213	71	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	462-463	212-213	71	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428860	17:7676039-7676039	CGGAAAC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	472-473	212-213	71	R/RFPX	cgt/cgGTTTCCGt	rs1131691004	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	452-471	310-329	104-110	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	310-329	310-329	104-110	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	310-329	310-329	104-110	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	443-462	310-329	104-110	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	446-465	310-329	104-110	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	443-462	310-329	104-110	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	492-511	310-329	104-110	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526565	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526565	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	566-585	-	-	-	-	rs1555526565	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	448-467	310-329	104-110	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526565	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526565	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526565	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526565	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=921;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526565	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2453;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	449-468	310-329	104-110	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	560-579	193-212	65-71	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	443-462	193-212	65-71	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526565	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526565	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526565	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	446-465	193-212	65-71	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	500-519	193-212	65-71	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	443-462	193-212	65-71	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
482225	17:7676039-7676059	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	453-472	193-212	65-71	QGSYGFR/X	CAGGGCAGCTACGGTTTCCGt/t	rs1555526565	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	471-472	329-330	110	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	329-330	329-330	110	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	329-330	329-330	110	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	462-463	329-330	110	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	465-466	329-330	110	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	462-463	329-330	110	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	511-512	329-330	110	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	585-586	-	-	-	-	rs1597373700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	467-468	329-330	110	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597373700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597373700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=920;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2452;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	468-469	329-330	110	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	579-580	212-213	71	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	462-463	212-213	71	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	465-466	212-213	71	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	519-520	212-213	71	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	462-463	212-213	71	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
641505	17:7676039-7676040	GG	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	472-473	212-213	71	R/P	cGT/cCC	rs1597373700	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	470	328	110	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	328	328	110	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	328	328	110	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	461	328	110	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	464	328	110	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	461	328	110	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	510	328	110	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	584	-	-	-	-	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	466	328	110	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=922;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2454;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	467	328	110	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	578	211	71	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	461	211	71	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	464	211	71	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	518	211	71	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	461	211	71	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
127807	17:7676040-7676041	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	471	211	71	R/X	Cgt/gt	rs587780066,CD136796,CD1617859,COSV105873667,COSV52684761,COSV53551526	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,0,1,1,1;PHENO=1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	471	329	110	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	329	329	110	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	329	329	110	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	462	329	110	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	465	329	110	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	462	329	110	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	511	329	110	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	585	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	467	329	110	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=921;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2453;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	468	329	110	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	579	212	71	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	462	212	71	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	465	212	71	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	519	212	71	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	462	212	71	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
406597	17:7676040-7676040	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	472	212	71	R/L	cGt/cTt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	469-470	327-328	109-110	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	327-328	327-328	109-110	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	327-328	327-328	109-110	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	460-461	327-328	109-110	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	463-464	327-328	109-110	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	460-461	327-328	109-110	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	509-510	327-328	109-110	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795434,COSV53611781	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795434,COSV53611781	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	583-584	-	-	-	-	rs1064795434,COSV53611781	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	465-466	327-328	109-110	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1064795434,COSV53611781	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795434,COSV53611781	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1064795434,COSV53611781	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795434,COSV53611781	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=922;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795434,COSV53611781	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2454;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	466-467	327-328	109-110	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	577-578	210-211	70-71	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	460-461	210-211	70-71	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795434,COSV53611781	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795434,COSV53611781	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795434,COSV53611781	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	463-464	210-211	70-71	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	517-518	210-211	70-71	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	460-461	210-211	70-71	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
421902	17:7676040-7676042	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	470-471	210-211	70-71	FR/LX	ttCCgt/ttgt	rs1064795434,COSV53611781	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	467-470	325-328	109-110	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	325-328	325-328	109-110	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	325-328	325-328	109-110	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	458-461	325-328	109-110	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	461-464	325-328	109-110	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	458-461	325-328	109-110	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	507-510	325-328	109-110	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373769	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373769	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	581-584	-	-	-	-	rs1597373769	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	463-466	325-328	109-110	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597373769	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373769	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597373769	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373769	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=922;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373769	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2454;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	464-467	325-328	109-110	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	575-578	208-211	70-71	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	458-461	208-211	70-71	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373769	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373769	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373769	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	461-464	208-211	70-71	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	515-518	208-211	70-71	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	458-461	208-211	70-71	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
823309	17:7676040-7676044	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	468-471	208-211	70-71	FR/X	TTCCgt/gt	rs1597373769	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	470-471	328-329	110	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	328-329	328-329	110	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	328-329	328-329	110	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	461-462	328-329	110	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	464-465	328-329	110	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	461-462	328-329	110	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	510-511	328-329	110	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104583344,COSV104588006,COSV53497694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104583344,COSV104588006,COSV53497694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	584-585	-	-	-	-	COSV104583344,COSV104588006,COSV53497694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	466-467	328-329	110	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV104583344,COSV104588006,COSV53497694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104583344,COSV104588006,COSV53497694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV104583344,COSV104588006,COSV53497694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104583344,COSV104588006,COSV53497694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=921;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104583344,COSV104588006,COSV53497694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2453;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	467-468	328-329	110	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	578-579	211-212	71	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	461-462	211-212	71	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104583344,COSV104588006,COSV53497694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104583344,COSV104588006,COSV53497694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104583344,COSV104588006,COSV53497694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	464-465	211-212	71	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	518-519	211-212	71	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	461-462	211-212	71	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
839197	17:7676040-7676040	GG	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	471-472	211-212	71	R/PX	cgt/cCCgt	COSV104583344,COSV104588006,COSV53497694	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	466-470	324-328	108-110	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	324-328	324-328	108-110	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	324-328	324-328	108-110	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	457-461	324-328	108-110	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	460-464	324-328	108-110	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	457-461	324-328	108-110	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	506-510	324-328	108-110	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691031,COSV53502172	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691031,COSV53502172	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	580-584	-	-	-	-	rs1131691031,COSV53502172	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	462-466	324-328	108-110	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1131691031,COSV53502172	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691031,COSV53502172	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1131691031,COSV53502172	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691031,COSV53502172	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=922;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691031,COSV53502172	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2454;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	463-467	324-328	108-110	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	574-578	207-211	69-71	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	457-461	207-211	69-71	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691031,COSV53502172	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691031,COSV53502172	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691031,COSV53502172	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=548;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	460-464	207-211	69-71	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	514-518	207-211	69-71	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	457-461	207-211	69-71	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428896	17:7676041-7676045	TTTT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	467-471	207-211	69-71	GFR/GKX	ggTTTCCgt/ggAAAAgt	rs1131691031,COSV53502172	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	462-469	320-327	107-109	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	320-327	320-327	107-109	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	320-327	320-327	107-109	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	453-460	320-327	107-109	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	456-463	320-327	107-109	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	453-460	320-327	107-109	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	502-509	320-327	107-109	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	576-583	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	458-465	320-327	107-109	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=923;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2455;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	459-466	320-327	107-109	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	570-577	203-210	68-70	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	453-460	203-210	68-70	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	456-463	203-210	68-70	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	510-517	203-210	68-70	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	453-460	203-210	68-70	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
945818	17:7676041-7676049	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	463-470	203-210	68-70	YGF/X	tACGGTTTC/t	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	468	326	109	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	326	326	109	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	326	326	109	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	459	326	109	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	462	326	109	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	459	326	109	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	508	326	109	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691038,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691038,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	582	-	-	-	-	rs1131691038,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	464	326	109	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1131691038,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691038,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1131691038,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691038,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=924;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691038,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2456;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	465	326	109	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	576	209	70	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	459	209	70	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691038,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691038,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691038,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	462	209	70	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	516	209	70	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	459	209	70	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428903	17:7676043-7676043	TTGGG	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	469	209	70	F/SQX	tTc/tCCCAAc	rs1131691038,COSV52725602,COSV52838438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	468	326	109	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	326	326	109	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	326	326	109	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	459	326	109	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	462	326	109	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	459	326	109	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	508	326	109	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	582	-	-	-	-	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	464	326	109	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=924;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2456;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	465	326	109	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	576	209	70	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	459	209	70	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	462	209	70	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	516	209	70	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	459	209	70	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634784	17:7676043-7676043	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	469	209	70	F/C	tTc/tGc	rs1064796722,COSV52725602,COSV52838438	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	467	325	109	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	325	325	109	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	325	325	109	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	458	325	109	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	461	325	109	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	458	325	109	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	507	325	109	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=551;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=551;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	581	-	-	-	-	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	463	325	109	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=551;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=925;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2457;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	464	325	109	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	575	208	70	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	458	208	70	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=551;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=551;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=551;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	461	208	70	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	515	208	70	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	458	208	70	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
389644	17:7676044-7676044	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	468	208	70	F/V	Ttc/Gtc	rs1057523496,COSV52819746,COSV53616876	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	456-466	314-324	105-108	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	314-324	314-324	105-108	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	314-324	314-324	105-108	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	447-457	314-324	105-108	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	450-460	314-324	105-108	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	447-457	314-324	105-108	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	496-506	314-324	105-108	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=552;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=552;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	570-580	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	452-462	314-324	105-108	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=552;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=926;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2458;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	453-463	314-324	105-108	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	564-574	197-207	66-69	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	447-457	197-207	66-69	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=552;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=552;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=552;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	450-460	197-207	66-69	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	504-514	197-207	66-69	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	447-457	197-207	66-69	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
965258	17:7676044-7676055	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	457-467	197-207	66-69	GSYG/X	gGCAGCTACGGT/g	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	465-466	323-324	108	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	323-324	323-324	108	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	323-324	323-324	108	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	456-457	323-324	108	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	459-460	323-324	108	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	456-457	323-324	108	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	505-506	323-324	108	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52690497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=552;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52690497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=552;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	579-580	-	-	-	-	COSV52690497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	461-462	323-324	108	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52690497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52690497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=552;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52690497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52690497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=926;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52690497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2458;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	462-463	323-324	108	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	573-574	206-207	69	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	456-457	206-207	69	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52690497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=552;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52690497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=552;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52690497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=552;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	459-460	206-207	69	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	513-514	206-207	69	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	456-457	206-207	69	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1675655	17:7676045-7676045	C	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	466-467	206-207	69	G/GX	ggt/ggGt	COSV52690497	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	463	321	107	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	321	321	107	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	321	321	107	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	454	321	107	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	457	321	107	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	454	321	107	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	503	321	107	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	577	-	-	-	-	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	459	321	107	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=929;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2461;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	460	321	107	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	571	204	68	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	454	204	68	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	457	204	68	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	511	204	68	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	454	204	68	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1073381	17:7676048-7676048	C	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	464	204	68	Y/*	taC/taG	CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	463	321	107	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	321	321	107	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	321	321	107	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	454	321	107	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	457	321	107	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	454	321	107	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	503	321	107	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	577	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	459	321	107	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=929;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2461;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	460	321	107	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	571	204	68	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	454	204	68	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	457	204	68	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	511	204	68	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	454	204	68	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406599	17:7676048-7676048	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	464	204	68	Y/*	taC/taA	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	456	314	105	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	314	314	105	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	314	314	105	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	447	314	105	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	450	314	105	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	447	314	105	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	496	314	105	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	570	-	-	-	-	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	452	314	105	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=936;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2468;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	453	314	105	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	564	197	66	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	447	197	66	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	450	197	66	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	504	197	66	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	447	197	66	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
592196	17:7676054-7676055	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	457	197	66	G/X	gGc/gc	rs1567555907,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	456	314	105	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	314	314	105	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	314	314	105	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	447	314	105	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	450	314	105	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	447	314	105	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	496	314	105	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	570	-	-	-	-	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	452	314	105	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=936;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2468;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	453	314	105	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	564	197	66	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	447	197	66	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	450	197	66	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	504	197	66	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	447	197	66	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634708	17:7676055-7676055	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	457	197	66	G/V	gGc/gTc	rs587781504,CM1617858,COSV52708806,COSV52766179,COSV52793434	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	455	313	105	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	313	313	105	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	313	313	105	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	446	313	105	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	449	313	105	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	446	313	105	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	495	313	105	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	569	-	-	-	-	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	451	313	105	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=937;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2469;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	452	313	105	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	563	196	66	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	446	196	66	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	449	196	66	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	503	196	66	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	446	196	66	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1802439	17:7676056-7676056	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	456	196	66	G/C	Ggc/Tgc	CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	455	313	105	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	313	313	105	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	313	313	105	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	446	313	105	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	449	313	105	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	446	313	105	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	495	313	105	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	569	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	451	313	105	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=937;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2469;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	452	313	105	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	563	196	66	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	446	196	66	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	449	196	66	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	503	196	66	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	446	196	66	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406574	17:7676056-7676056	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	456	196	66	G/R	Ggc/Cgc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	455	313	105	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	313	313	105	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	313	313	105	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	446	313	105	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	449	313	105	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	446	313	105	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	495	313	105	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	569	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	451	313	105	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=937;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2469;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	452	313	105	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	563	196	66	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	446	196	66	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=563;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	449	196	66	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	503	196	66	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	446	196	66	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428884	17:7676056-7676056	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	456	196	66	G/S	Ggc/Agc	rs1060501195,CM043949,COSV52726068,COSV52741717,COSV53015551	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	452	310	104	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	310	310	104	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	310	310	104	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	443	310	104	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	446	310	104	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	443	310	104	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	492	310	104	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555939,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555939,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	566	-	-	-	-	rs1567555939,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	448	310	104	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567555939,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555939,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567555939,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555939,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=940;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555939,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2472;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	449	310	104	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	560	193	65	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	443	193	65	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555939,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555939,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555939,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	446	193	65	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	500	193	65	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	443	193	65	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634663	17:7676058-7676059	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	453	193	65	Q/X	Cag/ag	rs1567555939,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	452	310	104	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	310	310	104	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	310	310	104	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	443	310	104	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	446	310	104	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	443	310	104	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	492	310	104	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555934,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555934,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	566	-	-	-	-	rs1567555934,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	448	310	104	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567555934,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555934,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567555934,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555934,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=940;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555934,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2472;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	449	310	104	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	560	193	65	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	443	193	65	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555934,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555934,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555934,COSV52694629	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	446	193	65	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	500	193	65	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	443	193	65	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
566924	17:7676059-7676059	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	453	193	65	Q/*	Cag/Tag	rs1567555934,COSV52694629	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	451	309	103	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	309	309	103	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	309	309	103	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	442	309	103	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	445	309	103	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	442	309	103	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	491	309	103	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=567;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=567;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	565	-	-	-	-	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	447	309	103	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=567;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=941;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2473;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	448	309	103	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	559	192	64	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	442	192	64	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=567;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=567;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=567;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	445	192	64	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	499	192	64	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	442	192	64	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
822878	17:7676060-7676060	C	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	452	192	64	Y/*	taC/taG	rs1597373901,CM073388,COSV52663474,COSV52761478,COSV52776039,COSV53023378	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	446-447	304-305	102	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	304-305	304-305	102	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	304-305	304-305	102	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	437-438	304-305	102	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	440-441	304-305	102	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	437-438	304-305	102	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	486-487	304-305	102	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=571;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=571;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	560-561	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	442-443	304-305	102	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=571;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=945;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2477;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	443-444	304-305	102	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	554-555	187-188	63	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	437-438	187-188	63	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=571;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=571;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=571;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	440-441	187-188	63	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	494-495	187-188	63	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	437-438	187-188	63	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396578	17:7676064-7676064	T	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	447-448	187-188	63	T/NX	acc/aAcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	446	304	102	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	304	304	102	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	304	304	102	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	437	304	102	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	440	304	102	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	437	304	102	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	486	304	102	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53305997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=572;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53305997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=572;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	560	-	-	-	-	COSV53305997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	442	304	102	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53305997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53305997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=572;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53305997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53305997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=946;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53305997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2478;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	443	304	102	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	554	187	63	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	437	187	63	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53305997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=572;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53305997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=572;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53305997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=572;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	440	187	63	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	494	187	63	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	437	187	63	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1799246	17:7676064-7676065	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	447	187	63	T/X	Acc/cc	COSV53305997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	436-440	294-298	98-100	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	294-298	294-298	98-100	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	294-298	294-298	98-100	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	427-431	294-298	98-100	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	430-434	294-298	98-100	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	427-431	294-298	98-100	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	476-480	294-298	98-100	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	550-554	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	432-436	294-298	98-100	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=952;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2484;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	433-437	294-298	98-100	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	544-548	177-181	59-61	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	427-431	177-181	59-61	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	430-434	177-181	59-61	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	484-488	177-181	59-61	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	427-431	177-181	59-61	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1332246	17:7676070-7676075	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	437-441	177-181	59-61	PSQ/PX	ccTTCCCag/ccag	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	440	298	100	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	298	298	100	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	298	298	100	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	431	298	100	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	434	298	100	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	431	298	100	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	480	298	100	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	554	-	-	-	-	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	436	298	100	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=952;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2484;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	437	298	100	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	548	181	61	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	431	181	61	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	434	181	61	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	488	181	61	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	431	181	61	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634674	17:7676070-7676071	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	441	181	61	Q/X	Cag/ag	rs1567556006,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	436-439	294-297	98-99	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	294-297	294-297	98-99	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	294-297	294-297	98-99	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	427-430	294-297	98-99	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	430-433	294-297	98-99	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	427-430	294-297	98-99	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	476-479	294-297	98-99	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=579;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=579;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	550-553	-	-	-	-	rs730882015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	432-435	294-297	98-99	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs730882015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=579;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs730882015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=953;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2485;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	433-436	294-297	98-99	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	544-547	177-180	59-60	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	427-430	177-180	59-60	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=579;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=579;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=579;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	430-433	177-180	59-60	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	484-487	177-180	59-60	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	427-430	177-180	59-60	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
182954	17:7676071-7676075	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	437-440	177-180	59-60	PS/X	ccTTCC/cc	rs730882015	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	440	298	100	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	298	298	100	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	298	298	100	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	431	298	100	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	434	298	100	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	431	298	100	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	480	298	100	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	554	-	-	-	-	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	436	298	100	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=952;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2484;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	437	298	100	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	548	181	61	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	431	181	61	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=578;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	434	181	61	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	488	181	61	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	431	181	61	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634707	17:7676071-7676071	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	441	181	61	Q/*	Cag/Tag	rs1567555994,CM156961,COSV52702138,COSV53867973	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	437	295	99	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	295	295	99	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	295	295	99	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	428	295	99	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	431	295	99	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	428	295	99	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	477	295	99	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526593,COSV53312510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=581;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526593,COSV53312510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=581;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	551	-	-	-	-	rs1555526593,COSV53312510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	433	295	99	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526593,COSV53312510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526593,COSV53312510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=581;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526593,COSV53312510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526593,COSV53312510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=955;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526593,COSV53312510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2487;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	434	295	99	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	545	178	60	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	428	178	60	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526593,COSV53312510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=581;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526593,COSV53312510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=581;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526593,COSV53312510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=581;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	431	178	60	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	485	178	60	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	428	178	60	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528244	17:7676073-7676074	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	438	178	60	S/X	Tcc/cc	rs1555526593,COSV53312510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	426-430	284-288	95-96	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	284-288	284-288	95-96	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	284-288	284-288	95-96	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	417-421	284-288	95-96	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	420-424	284-288	95-96	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	417-421	284-288	95-96	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	466-470	284-288	95-96	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	540-544	-	-	-	-	rs878854068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	422-426	284-288	95-96	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs878854068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs878854068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=962;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2494;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	423-427	284-288	95-96	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	534-538	167-171	56-57	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	417-421	167-171	56-57	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	420-424	167-171	56-57	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	474-478	167-171	56-57	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	417-421	167-171	56-57	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
634703	17:7676080-7676085	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	427-431	167-171	56-57	SS/X	tCTTCT/t	rs878854068	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	423	281	94	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	281	281	94	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	281	281	94	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	414	281	94	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	417	281	94	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	414	281	94	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	463	281	94	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=595;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=595;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	537	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	419	281	94	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=595;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=969;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2501;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	420	281	94	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	531	164	55	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	414	164	55	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=595;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=595;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=595;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	417	164	55	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	471	164	55	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	414	164	55	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796419	17:7676088-7676088	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	424	164	55	S/*	tCa/tAa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	399-421	257-279	86-93	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	257-279	257-279	86-93	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	257-279	257-279	86-93	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	390-412	257-279	86-93	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	393-415	257-279	86-93	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	390-412	257-279	86-93	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	439-461	257-279	86-93	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs886041861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs886041861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	513-535	-	-	-	-	rs886041861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	395-417	257-279	86-93	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs886041861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs886041861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs886041861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs886041861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs886041861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2503;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	396-418	257-279	86-93	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	507-529	140-162	47-54	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	390-412	140-162	47-54	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs886041861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs886041861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs886041861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	393-415	140-162	47-54	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	447-469	140-162	47-54	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	390-412	140-162	47-54	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
280704	17:7676089-7676112	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	400-422	140-162	47-54	APAPSWPL/X	gCACCAGCCCCCTCCTGGCCCCTG/g	rs886041861	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	415-421	273-279	91-93	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	273-279	273-279	91-93	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	273-279	273-279	91-93	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	406-412	273-279	91-93	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	409-415	273-279	91-93	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	406-412	273-279	91-93	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	455-461	273-279	91-93	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796124	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796124	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	529-535	-	-	-	-	rs1064796124	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	411-417	273-279	91-93	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1064796124	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796124	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1064796124	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796124	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796124	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2503;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	412-418	273-279	91-93	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	523-529	156-162	52-54	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	406-412	156-162	52-54	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796124	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796124	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796124	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	409-415	156-162	52-54	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	463-469	156-162	52-54	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	406-412	156-162	52-54	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
422961	17:7676089-7676096	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	416-422	156-162	52-54	WPL/X	tgGCCCCTG/tg	rs1064796124	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	369-421	227-279	76-93	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	227-279	227-279	76-93	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	227-279	227-279	76-93	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	360-412	227-279	76-93	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	363-415	227-279	76-93	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	360-412	227-279	76-93	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	409-461	227-279	76-93	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	483-535	-	-	-	-	rs1555526610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	365-417	227-279	76-93	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2503;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	366-418	227-279	76-93	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	477-529	110-162	37-54	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	360-412	110-162	37-54	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	363-415	110-162	37-54	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	417-469	110-162	37-54	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	360-412	110-162	37-54	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428858	17:7676089-7676142	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	370-422	110-162	37-54	APAAPTPAAPAPAPSWPL/X	gCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTG/g	rs1555526610	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	420-421	278-279	93	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	278-279	278-279	93	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	278-279	278-279	93	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	411-412	278-279	93	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	414-415	278-279	93	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	411-412	278-279	93	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	460-461	278-279	93	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99478158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99478158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	534-535	-	-	-	-	COSV99478158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	416-417	278-279	93	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV99478158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99478158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV99478158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99478158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99478158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2503;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	417-418	278-279	93	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	528-529	161-162	54	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	411-412	161-162	54	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99478158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99478158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99478158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	414-415	161-162	54	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	468-469	161-162	54	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	411-412	161-162	54	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1074584	17:7676090-7676090	AGAAGGAAGGGACAGAAGGA	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	421-422	161-162	54	L/LPSVPSFX	ctg/ctTCCTTCTGTCCCTTCCTTCTg	COSV99478158	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	420	278	93	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	278	278	93	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	278	278	93	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	411	278	93	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	414	278	93	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	411	278	93	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	460	278	93	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556114,COSV53344875	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=598;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556114,COSV53344875	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=598;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	534	-	-	-	-	rs1567556114,COSV53344875	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	416	278	93	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567556114,COSV53344875	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556114,COSV53344875	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=598;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567556114,COSV53344875	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556114,COSV53344875	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556114,COSV53344875	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2504;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	417	278	93	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	528	161	54	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	411	161	54	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556114,COSV53344875	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=598;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556114,COSV53344875	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=598;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556114,COSV53344875	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=598;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	414	161	54	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	468	161	54	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	411	161	54	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634689	17:7676090-7676091	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	421	161	54	L/X	cTg/cg	rs1567556114,COSV53344875	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	419-420	277-278	93	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	277-278	277-278	93	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	277-278	277-278	93	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	410-411	277-278	93	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	413-414	277-278	93	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	410-411	277-278	93	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	459-460	277-278	93	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374098,COSV52989547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=598;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374098,COSV52989547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=598;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	533-534	-	-	-	-	rs1597374098,COSV52989547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	415-416	277-278	93	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597374098,COSV52989547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374098,COSV52989547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=598;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597374098,COSV52989547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374098,COSV52989547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374098,COSV52989547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2504;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	416-417	277-278	93	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	527-528	160-161	54	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	410-411	160-161	54	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374098,COSV52989547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=598;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374098,COSV52989547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=598;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374098,COSV52989547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=598;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	413-414	160-161	54	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	467-468	160-161	54	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	410-411	160-161	54	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
821781	17:7676090-7676092	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	420-421	160-161	54	L/X	CTg/g	rs1597374098,COSV52989547	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	419	277	93	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	277	277	93	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	277	277	93	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	410	277	93	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	413	277	93	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	410	277	93	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	459	277	93	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556123,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556123,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	533	-	-	-	-	rs1567556123,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	415	277	93	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567556123,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556123,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567556123,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556123,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=973;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556123,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2505;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	416	277	93	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	527	160	54	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	410	160	54	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556123,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556123,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556123,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	413	160	54	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	467	160	54	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	410	160	54	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634692	17:7676091-7676092	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	420	160	54	L/X	Ctg/tg	rs1567556123,COSV53525400	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	415	273	91	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	273	273	91	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	273	273	91	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	406	273	91	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	409	273	91	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	406	273	91	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	455	273	91	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660548,CM065495,COSV52673580	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=603;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660548,CM065495,COSV52673580	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=603;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	529	-	-	-	-	rs876660548,CM065495,COSV52673580	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	411	273	91	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876660548,CM065495,COSV52673580	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660548,CM065495,COSV52673580	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=603;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs876660548,CM065495,COSV52673580	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660548,CM065495,COSV52673580	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=977;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660548,CM065495,COSV52673580	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2509;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	412	273	91	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	523	156	52	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	406	156	52	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660548,CM065495,COSV52673580	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=603;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660548,CM065495,COSV52673580	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=603;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660548,CM065495,COSV52673580	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=603;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	409	156	52	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	463	156	52	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	406	156	52	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
233650	17:7676096-7676096	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	416	156	52	W/*	tgG/tgA	rs876660548,CM065495,COSV52673580	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	413-414	271-272	91	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	271-272	271-272	91	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	271-272	271-272	91	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	404-405	271-272	91	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	407-408	271-272	91	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	404-405	271-272	91	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	453-454	271-272	91	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374152,COSV53428420,COSV99369937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374152,COSV53428420,COSV99369937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	527-528	-	-	-	-	rs1597374152,COSV53428420,COSV99369937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	409-410	271-272	91	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597374152,COSV53428420,COSV99369937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374152,COSV53428420,COSV99369937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597374152,COSV53428420,COSV99369937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374152,COSV53428420,COSV99369937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=978;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374152,COSV53428420,COSV99369937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2510;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	410-411	271-272	91	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	521-522	154-155	52	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	404-405	154-155	52	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374152,COSV53428420,COSV99369937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374152,COSV53428420,COSV99369937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374152,COSV53428420,COSV99369937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	407-408	154-155	52	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	461-462	154-155	52	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	404-405	154-155	52	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
801291	17:7676097-7676097	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	414-415	154-155	52	W/LX	tgg/tTgg	rs1597374152,COSV53428420,COSV99369937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	414	272	91	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	272	272	91	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	272	272	91	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	405	272	91	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	408	272	91	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	405	272	91	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	454	272	91	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073465664,COSV52734595,COSV53139118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073465664,COSV52734595,COSV53139118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	528	-	-	-	-	rs2073465664,COSV52734595,COSV53139118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	410	272	91	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs2073465664,COSV52734595,COSV53139118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073465664,COSV52734595,COSV53139118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs2073465664,COSV52734595,COSV53139118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073465664,COSV52734595,COSV53139118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=978;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073465664,COSV52734595,COSV53139118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2510;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	411	272	91	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	522	155	52	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	405	155	52	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073465664,COSV52734595,COSV53139118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073465664,COSV52734595,COSV53139118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073465664,COSV52734595,COSV53139118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=604;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	408	155	52	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	462	155	52	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	405	155	52	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
979079	17:7676097-7676097	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	415	155	52	W/*	tGg/tAg	rs2073465664,COSV52734595,COSV53139118	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	403-412	261-270	87-90	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	261-270	261-270	87-90	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	261-270	261-270	87-90	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	394-403	261-270	87-90	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	397-406	261-270	87-90	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	394-403	261-270	87-90	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	443-452	261-270	87-90	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	517-526	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	399-408	261-270	87-90	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=980;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2512;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	400-409	261-270	87-90	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	511-520	144-153	48-51	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	394-403	144-153	48-51	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	397-406	144-153	48-51	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	451-460	144-153	48-51	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	394-403	144-153	48-51	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1793790	17:7676098-7676108	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	404-413	144-153	48-51	PAPS/X	ccAGCCCCCTCC/cc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	402-412	260-270	87-90	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	260-270	260-270	87-90	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	260-270	260-270	87-90	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	393-403	260-270	87-90	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	396-406	260-270	87-90	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	393-403	260-270	87-90	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	442-452	260-270	87-90	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	516-526	-	-	-	-	rs1567556165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	398-408	260-270	87-90	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567556165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567556165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=980;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2512;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	399-409	260-270	87-90	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	510-520	143-153	48-51	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	393-403	143-153	48-51	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	396-406	143-153	48-51	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	450-460	143-153	48-51	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	393-403	143-153	48-51	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634750	17:7676098-7676109	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	403-413	143-153	48-51	PAPS/X	cCAGCCCCCTCC/c	rs1567556165	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	410-411	268-269	90	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	268-269	268-269	90	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	268-269	268-269	90	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	401-402	268-269	90	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	404-405	268-269	90	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	401-402	268-269	90	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	450-451	268-269	90	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=607;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=607;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	524-525	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	406-407	268-269	90	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=607;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=981;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2513;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	407-408	268-269	90	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	518-519	151-152	51	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	401-402	151-152	51	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=607;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=607;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=607;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	404-405	151-152	51	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	458-459	151-152	51	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	401-402	151-152	51	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1069253	17:7676100-7676100	AGGGGCAGGGGCAGGGGCCAGGAGGGGC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	411-412	151-152	51	S/CPSWPLPLPLX	tcc/tGCCCCTCCTGGCCCCTGCCCCTGCCCCTcc	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	409	267	89	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	267	267	89	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	267	267	89	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	400	267	89	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	403	267	89	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	400	267	89	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	449	267	89	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	523	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	405	267	89	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=983;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2515;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	406	267	89	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	517	150	50	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	400	150	50	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	403	150	50	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	457	150	50	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	400	150	50	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
156515	17:7676101-7676102	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	410	150	50	P/X	ccC/cc	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	409-410	267-268	89-90	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	267-268	267-268	89-90	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	267-268	267-268	89-90	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	400-401	267-268	89-90	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	403-404	267-268	89-90	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	400-401	267-268	89-90	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	449-450	267-268	89-90	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=608;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=608;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	523-524	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	405-406	267-268	89-90	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=608;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2514;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	406-407	267-268	89-90	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	517-518	150-151	50-51	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	400-401	150-151	50-51	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=608;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=608;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587783062	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=608;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	403-404	150-151	50-51	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	457-458	150-151	50-51	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	400-401	150-151	50-51	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
634762	17:7676101-7676101	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	410-411	150-151	50-51	-/X	-/C	rs587783062	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	404	262	88	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	262	262	88	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	262	262	88	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	395	262	88	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	398	262	88	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	395	262	88	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	444	262	88	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53134951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=614;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53134951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=614;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	518	-	-	-	-	COSV53134951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	400	262	88	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53134951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53134951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=614;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53134951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53134951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=988;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53134951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2520;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	401	262	88	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	512	145	49	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	395	145	49	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53134951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=614;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53134951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=614;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53134951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=614;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	398	145	49	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	452	145	49	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	395	145	49	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1363662	17:7676106-7676107	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	405	145	49	A/X	Gcc/cc	COSV53134951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	389-398	247-256	83-86	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	247-256	247-256	83-86	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	247-256	247-256	83-86	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	380-389	247-256	83-86	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	383-392	247-256	83-86	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	380-389	247-256	83-86	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	429-438	247-256	83-86	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526635	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526635	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	503-512	-	-	-	-	rs1555526635	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	385-394	247-256	83-86	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526635	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526635	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526635	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526635	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=994;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526635	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2526;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	386-395	247-256	83-86	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	497-506	130-139	44-47	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	380-389	130-139	44-47	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526635	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526635	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526635	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	383-392	130-139	44-47	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	437-446	130-139	44-47	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	380-389	130-139	44-47	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
545773	17:7676112-7676122	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	390-399	130-139	44-47	AAPA/X	GCGGCCCCTGca/ca	rs1555526635	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	396-397	254-255	85	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	254-255	254-255	85	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	254-255	254-255	85	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	387-388	254-255	85	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	390-391	254-255	85	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	387-388	254-255	85	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	436-437	254-255	85	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104581950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104581950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	510-511	-	-	-	-	COSV104581950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	392-393	254-255	85	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV104581950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104581950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV104581950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104581950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=995;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104581950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2527;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	393-394	254-255	85	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	504-505	137-138	46	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	387-388	137-138	46	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104581950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104581950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104581950	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	390-391	137-138	46	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	444-445	137-138	46	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	387-388	137-138	46	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1400022	17:7676114-7676114	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	397-398	137-138	46	P/PX	cct/ccCt	COSV104581950	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	396	254	85	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	254	254	85	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	254	254	85	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	387	254	85	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	390	254	85	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	387	254	85	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	436	254	85	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064793279,COSV53087170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=622;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064793279,COSV53087170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=622;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	510	-	-	-	-	rs1064793279,COSV53087170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	392	254	85	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1064793279,COSV53087170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064793279,COSV53087170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=622;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1064793279,COSV53087170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064793279,COSV53087170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=996;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064793279,COSV53087170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2528;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	393	254	85	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	504	137	46	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	387	137	46	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064793279,COSV53087170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=622;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064793279,COSV53087170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=622;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064793279,COSV53087170	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=622;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	390	137	46	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	444	137	46	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	387	137	46	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
418516	17:7676114-7676115	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	397	137	46	P/X	cCt/ct	rs1064793279,COSV53087170	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	388-395	246-253	82-85	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	246-253	246-253	82-85	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	246-253	246-253	82-85	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	379-386	246-253	82-85	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	382-389	246-253	82-85	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	379-386	246-253	82-85	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	428-435	246-253	82-85	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=623;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=623;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	502-509	-	-	-	-	rs1567556270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	384-391	246-253	82-85	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567556270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=623;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567556270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=997;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2529;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	385-392	246-253	82-85	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	496-503	129-136	43-46	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	379-386	129-136	43-46	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=623;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=623;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=623;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	382-389	129-136	43-46	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	436-443	129-136	43-46	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	379-386	129-136	43-46	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634758	17:7676115-7676123	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	389-396	129-136	43-46	PAAP/PX	ccGGCGGCCCct/ccct	rs1567556270	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	392	250	84	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	250	250	84	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	250	250	84	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	383	250	84	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	386	250	84	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	383	250	84	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	432	250	84	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374343,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374343,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	506	-	-	-	-	rs1597374343,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	388	250	84	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597374343,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374343,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597374343,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374343,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1000;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374343,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2532;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	389	250	84	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	500	133	45	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	383	133	45	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374343,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374343,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374343,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	386	133	45	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	440	133	45	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	383	133	45	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
646068	17:7676118-7676119	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	393	133	45	A/X	Gcc/cc	rs1597374343,COSV53077353	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	390-391	248-249	83	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	248-249	248-249	83	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	248-249	248-249	83	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	381-382	248-249	83	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	384-385	248-249	83	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	381-382	248-249	83	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	430-431	248-249	83	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	504-505	-	-	-	-	rs1131691010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	386-387	248-249	83	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1131691010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1131691010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1001;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2533;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	387-388	248-249	83	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	498-499	131-132	44	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	381-382	131-132	44	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	384-385	131-132	44	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	438-439	131-132	44	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	381-382	131-132	44	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428869	17:7676119-7676121	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	391-392	131-132	44	A/X	gCG/g	rs1131691010	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	389	247	83	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	247	247	83	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	247	247	83	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	380	247	83	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	383	247	83	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	380	247	83	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	429	247	83	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs867725248,COSV104370331	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=629;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs867725248,COSV104370331	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=629;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	503	-	-	-	-	rs867725248,COSV104370331	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	385	247	83	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs867725248,COSV104370331	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs867725248,COSV104370331	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=629;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs867725248,COSV104370331	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs867725248,COSV104370331	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1003;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs867725248,COSV104370331	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2535;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	386	247	83	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	497	130	44	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	380	130	44	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs867725248,COSV104370331	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=629;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs867725248,COSV104370331	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=629;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs867725248,COSV104370331	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=629;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	383	130	44	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	437	130	44	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	380	130	44	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634686	17:7676121-7676122	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	390	130	44	A/X	Gcg/cg	rs867725248,COSV104370331	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	387	245	82	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	245	245	82	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	245	245	82	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	378	245	82	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	381	245	82	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	378	245	82	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	427	245	82	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	501	-	-	-	-	CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	383	245	82	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1005;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2537;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	384	245	82	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	495	128	43	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	378	128	43	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	381	128	43	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	435	128	43	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	378	128	43	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1071800	17:7676123-7676124	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	388	128	43	P/X	cCg/cg	CM961375,COSV53209087	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	386-387	244-245	82	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	244-245	244-245	82	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	244-245	244-245	82	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	377-378	244-245	82	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	380-381	244-245	82	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	377-378	244-245	82	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	426-427	244-245	82	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	500-501	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	382-383	244-245	82	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1005;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2537;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	383-384	244-245	82	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	494-495	127-128	43	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	377-378	127-128	43	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	380-381	127-128	43	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	434-435	127-128	43	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	377-378	127-128	43	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1454088	17:7676124-7676124	GTGTAGGAGCTGCTGGT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	387-388	127-128	43	P/HQQLLHX	ccg/cACCAGCAGCTCCTACACcg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	383-384	241-242	81	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	241-242	241-242	81	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	241-242	241-242	81	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	374-375	241-242	81	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	377-378	241-242	81	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	374-375	241-242	81	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	423-424	241-242	81	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=634;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=634;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	497-498	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	379-380	241-242	81	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=634;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1008;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2540;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	380-381	241-242	81	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	491-492	124-125	42	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	374-375	124-125	42	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=634;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=634;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=634;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	377-378	124-125	42	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	431-432	124-125	42	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	374-375	124-125	42	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
947100	17:7676127-7676127	T	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	384-385	124-125	42	T/NX	aca/aAca	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	369-370	227-228	76	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	227-228	227-228	76	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	227-228	227-228	76	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	360-361	227-228	76	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	363-364	227-228	76	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	360-361	227-228	76	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	409-410	227-228	76	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	483-484	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	365-366	227-228	76	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1022;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2554;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	366-367	227-228	76	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	477-478	110-111	37	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	360-361	110-111	37	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	363-364	110-111	37	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	417-418	110-111	37	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	360-361	110-111	37	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1420489	17:7676141-7676141	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	370-371	110-111	37	A/AX	gca/gcCa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	366	224	75	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	224	224	75	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	224	224	75	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	357	224	75	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	360	224	75	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	357	224	75	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	406	224	75	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53349944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=652;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53349944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=652;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	480	-	-	-	-	COSV53349944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	362	224	75	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53349944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53349944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=652;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53349944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53349944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1026;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53349944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2558;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	363	224	75	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	474	107	36	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	357	107	36	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53349944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=652;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53349944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=652;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53349944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=652;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	360	107	36	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	414	107	36	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	357	107	36	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1396062	17:7676144-7676145	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	367	107	36	P/X	cCt/ct	COSV53349944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	366-367	224-225	75	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	224-225	224-225	75	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	224-225	224-225	75	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	357-358	224-225	75	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	360-361	224-225	75	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	357-358	224-225	75	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	406-407	224-225	75	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556454,COSV52714946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=651;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556454,COSV52714946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=651;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	480-481	-	-	-	-	rs1567556454,COSV52714946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	362-363	224-225	75	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567556454,COSV52714946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556454,COSV52714946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=651;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567556454,COSV52714946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556454,COSV52714946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1025;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556454,COSV52714946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2557;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	363-364	224-225	75	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	474-475	107-108	36	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	357-358	107-108	36	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556454,COSV52714946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=651;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556454,COSV52714946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=651;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556454,COSV52714946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=651;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	360-361	107-108	36	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	414-415	107-108	36	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	357-358	107-108	36	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634748	17:7676144-7676144	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	367-368	107-108	36	P/PX	cct/ccCt	rs1567556454,COSV52714946	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	358-359	216-217	72-73	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	216-217	216-217	72-73	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	216-217	216-217	72-73	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	349-350	216-217	72-73	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	352-353	216-217	72-73	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	349-350	216-217	72-73	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	398-399	216-217	72-73	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104369723	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104369723	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	472-473	-	-	-	-	rs730882018,COSV104369723	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	354-355	216-217	72-73	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs730882018,COSV104369723	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104369723	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs730882018,COSV104369723	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104369723	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1033;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104369723	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2565;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	355-356	216-217	72-73	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	466-467	99-100	33-34	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	349-350	99-100	33-34	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104369723	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104369723	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104369723	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	352-353	99-100	33-34	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	406-407	99-100	33-34	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	349-350	99-100	33-34	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
182957	17:7676152-7676152	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	359-360	99-100	33-34	-/X	-/C	rs730882018,COSV104369723	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	358	216	72	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	216	216	72	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	216	216	72	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	349	216	72	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	352	216	72	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	349	216	72	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	398	216	72	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	472	-	-	-	-	rs730882018,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	354	216	72	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs730882018,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs730882018,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1034;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2566;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	355	216	72	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	466	99	33	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	349	99	33	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882018,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	352	99	33	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	406	99	33	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	349	99	33	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428897	17:7676152-7676153	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	359	99	33	P/X	ccC/cc	rs730882018,COSV104586728	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic,pathogenic;SOMATIC=0,1;PHENO=1,1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	356-357	214-215	72	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	214-215	214-215	72	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	214-215	214-215	72	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	347-348	214-215	72	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	350-351	214-215	72	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	347-348	214-215	72	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	396-397	214-215	72	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	470-471	-	-	-	-	rs1131691014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	352-353	214-215	72	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1131691014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1131691014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1035;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2567;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	353-354	214-215	72	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	464-465	97-98	33	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	347-348	97-98	33	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	350-351	97-98	33	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	404-405	97-98	33	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	347-348	97-98	33	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428874	17:7676154-7676154	C	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	357-358	97-98	33	P/RX	ccc/cGcc	rs1131691014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	347	205	69	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	205	205	69	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	205	205	69	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	338	205	69	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	341	205	69	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	338	205	69	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	387	205	69	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=671;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=671;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	461	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	343	205	69	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=671;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1045;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2577;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	344	205	69	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	455	88	30	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	338	88	30	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=671;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=671;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=671;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	341	88	30	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	395	88	30	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	338	88	30	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1070469	17:7676163-7676164	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	348	88	30	A/X	Gct/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	344	202	68	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	202	202	68	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	202	202	68	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	335	202	68	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	338	202	68	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	335	202	68	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	384	202	68	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=674;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=674;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	458	-	-	-	-	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	340	202	68	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=674;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1048;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2580;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	341	202	68	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	452	85	29	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	335	85	29	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=674;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=674;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=674;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	338	85	29	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	392	85	29	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	335	85	29	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
224551	17:7676167-7676167	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	345	85	29	E/*	Gag/Tag	rs869312782,COSV52692559,COSV52721885,COSV53153630,COSV53758203	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	342	200	67	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	200	200	67	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	200	200	67	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	333	200	67	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	336	200	67	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	333	200	67	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	382	200	67	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52994866,COSV53267749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=676;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52994866,COSV53267749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=676;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	456	-	-	-	-	COSV52994866,COSV53267749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	338	200	67	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52994866,COSV53267749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52994866,COSV53267749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=676;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52994866,COSV53267749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52994866,COSV53267749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1050;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52994866,COSV53267749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2582;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	339	200	67	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	450	83	28	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	333	83	28	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52994866,COSV53267749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=676;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52994866,COSV53267749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=676;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52994866,COSV53267749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=676;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	336	83	28	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	390	83	28	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	333	83	28	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1784383	17:7676168-7676169	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	343	83	28	P/X	cCa/ca	COSV52994866,COSV53267749	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	338-339	196-197	66	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	196-197	196-197	66	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	196-197	196-197	66	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	329-330	196-197	66	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	332-333	196-197	66	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	329-330	196-197	66	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	378-379	196-197	66	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374735,COSV53099344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=679;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374735,COSV53099344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=679;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	452-453	-	-	-	-	rs1597374735,COSV53099344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	334-335	196-197	66	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597374735,COSV53099344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374735,COSV53099344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=679;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597374735,COSV53099344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374735,COSV53099344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1053;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374735,COSV53099344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2585;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	335-336	196-197	66	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	446-447	79-80	27	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	329-330	79-80	27	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374735,COSV53099344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=679;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374735,COSV53099344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=679;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374735,COSV53099344	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=679;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	332-333	79-80	27	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	386-387	79-80	27	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	329-330	79-80	27	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
650963	17:7676172-7676172	T	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	339-340	79-80	27	M/NX	atg/aAtg	rs1597374735,COSV53099344	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	335	193	65	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	193	193	65	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	193	193	65	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	326	193	65	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	329	193	65	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	326	193	65	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	375	193	65	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	449	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	331	193	65	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2589;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	332	193	65	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	443	76	26	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	326	76	26	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	329	76	26	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	383	76	26	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	326	76	26	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634670	17:7676176-7676176	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	336	76	26	R/*	Aga/Tga	rs1555526721,COSV52689560	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	326	184	62	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	184	184	62	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	184	184	62	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	317	184	62	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	320	184	62	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	317	184	62	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	366	184	62	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=692;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=692;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	440	-	-	-	-	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	322	184	62	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=692;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1066;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2598;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	323	184	62	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	434	67	23	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	317	67	23	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=692;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=692;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=692;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	320	67	23	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	374	67	23	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	317	67	23	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
617472	17:7676185-7676185	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	327	67	23	E/*	Gaa/Taa	rs1567556752,CM120852,COSV52811974,COSV52991347	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	318	176	59	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	176	176	59	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	176	176	59	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	309	176	59	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	312	176	59	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	309	176	59	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	358	176	59	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556784,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=700;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556784,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=700;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	432	-	-	-	-	rs1567556784,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	314	176	59	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567556784,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556784,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=700;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567556784,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556784,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556784,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2606;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	315	176	59	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	426	59	20	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	309	59	20	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556784,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=700;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556784,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=700;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556784,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=700;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	312	59	20	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	366	59	20	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	309	59	20	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634691	17:7676192-7676193	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	319	59	20	G/X	gGt/gt	rs1567556784,COSV53624897	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	315	173	58	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	173	173	58	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	173	173	58	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	306	173	58	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	309	173	58	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	306	173	58	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	355	173	58	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52675650,COSV53041942,COSV53097051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=703;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52675650,COSV53041942,COSV53097051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=703;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	429	-	-	-	-	COSV52675650,COSV53041942,COSV53097051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	311	173	58	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52675650,COSV53041942,COSV53097051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52675650,COSV53041942,COSV53097051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=703;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52675650,COSV53041942,COSV53097051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52675650,COSV53041942,COSV53097051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1077;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52675650,COSV53041942,COSV53097051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2609;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	312	173	58	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	423	56	19	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	306	56	19	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52675650,COSV53041942,COSV53097051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=703;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52675650,COSV53041942,COSV53097051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=703;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52675650,COSV53041942,COSV53097051	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=703;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	309	56	19	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	363	56	19	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	306	56	19	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1394451	17:7676195-7676196	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	316	56	19	P/X	cCa/ca	COSV52675650,COSV53041942,COSV53097051	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	308	166	56	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	166	166	56	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	166	166	56	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	299	166	56	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	302	166	56	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	299	166	56	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	348	166	56	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52771366,COSV52826932,COSV52883452	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=710;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52771366,COSV52826932,COSV52883452	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=710;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	422	-	-	-	-	COSV52771366,COSV52826932,COSV52883452	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	304	166	56	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52771366,COSV52826932,COSV52883452	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52771366,COSV52826932,COSV52883452	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=710;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52771366,COSV52826932,COSV52883452	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52771366,COSV52826932,COSV52883452	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1084;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52771366,COSV52826932,COSV52883452	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2616;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	305	166	56	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	416	49	17	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	299	49	17	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52771366,COSV52826932,COSV52883452	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=710;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52771366,COSV52826932,COSV52883452	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=710;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52771366,COSV52826932,COSV52883452	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=710;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	302	49	17	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	356	49	17	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	299	49	17	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1329425	17:7676203-7676203	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	309	49	17	E/*	Gaa/Taa	COSV52771366,COSV52826932,COSV52883452	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	297-306	155-164	52-55	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	155-164	155-164	52-55	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	155-164	155-164	52-55	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	288-297	155-164	52-55	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	291-300	155-164	52-55	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	288-297	155-164	52-55	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	337-346	155-164	52-55	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=712;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=712;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	411-420	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	293-302	155-164	52-55	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=712;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1086;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2618;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	294-303	155-164	52-55	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	405-414	38-47	13-16	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	288-297	38-47	13-16	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=712;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=712;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=712;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	291-300	38-47	13-16	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	345-354	38-47	13-16	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	288-297	38-47	13-16	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775035	17:7676204-7676214	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	298-307	38-47	13-16	QWFT/X	cAATGGTTCACt/ct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	304	162	54	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	162	162	54	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	162	162	54	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	295	162	54	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	298	162	54	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	295	162	54	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	344	162	54	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53252516,COSV53579173,COSV53821753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=714;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53252516,COSV53579173,COSV53821753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=714;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	418	-	-	-	-	COSV53252516,COSV53579173,COSV53821753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	300	162	54	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53252516,COSV53579173,COSV53821753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53252516,COSV53579173,COSV53821753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=714;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53252516,COSV53579173,COSV53821753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53252516,COSV53579173,COSV53821753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1088;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53252516,COSV53579173,COSV53821753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2620;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	301	162	54	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	412	45	15	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	295	45	15	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53252516,COSV53579173,COSV53821753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=714;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53252516,COSV53579173,COSV53821753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=714;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53252516,COSV53579173,COSV53821753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=714;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	298	45	15	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	352	45	15	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	295	45	15	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1452298	17:7676206-7676207	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	305	45	15	F/X	ttC/tt	COSV53252516,COSV53579173,COSV53821753	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	300-305	158-163	53-55	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	158-163	158-163	53-55	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	158-163	158-163	53-55	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	291-296	158-163	53-55	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	294-299	158-163	53-55	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	291-296	158-163	53-55	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	340-345	158-163	53-55	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=713;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=713;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	414-419	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	296-301	158-163	53-55	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=713;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1087;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2619;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	297-302	158-163	53-55	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	408-413	41-46	14-16	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	291-296	41-46	14-16	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=713;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=713;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=713;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	294-299	41-46	14-16	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	348-353	41-46	14-16	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	291-296	41-46	14-16	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679017	17:7676206-7676211	AT	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	301-306	41-46	14-16	WFT/YX	tGGTTCAct/tATct	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	300-301	158-159	53	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	158-159	158-159	53	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	158-159	158-159	53	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	291-292	158-159	53	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	294-295	158-159	53	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	291-292	158-159	53	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	340-341	158-159	53	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	414-415	-	-	-	-	COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	296-297	158-159	53	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1091;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2623;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	297-298	158-159	53	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	408-409	41-42	14	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	291-292	41-42	14	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	294-295	41-42	14	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	348-349	41-42	14	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	291-292	41-42	14	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775238	17:7676210-7676210	CAT	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	301-302	41-42	14	W/*W	tgg/tgATGg	COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	301	159	53	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	159	159	53	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	159	159	53	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	292	159	53	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	295	159	53	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	292	159	53	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	341	159	53	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	415	-	-	-	-	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	297	159	53	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1091;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2623;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	298	159	53	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	409	42	14	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	292	42	14	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	295	42	14	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	349	42	14	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	292	42	14	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
420659	17:7676210-7676210	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	302	42	14	W/*	tgG/tgA	rs1064794618,COSV52751414,COSV53223969,COSV53499187	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1;PHENO=1,1,1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained,frameshift_variant	300-301	158-159	53	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained,frameshift_variant	158-159	158-159	53	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained,frameshift_variant	158-159	158-159	53	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained,frameshift_variant	291-292	158-159	53	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained,frameshift_variant	294-295	158-159	53	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained,frameshift_variant	291-292	158-159	53	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained,frameshift_variant	340-341	158-159	53	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1195793509,COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1195793509,COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	414-415	-	-	-	-	rs1195793509,COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained,frameshift_variant	296-297	158-159	53	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1195793509,COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1195793509,COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1195793509,COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1195793509,COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1091;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1195793509,COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2623;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained,frameshift_variant	297-298	158-159	53	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained,frameshift_variant	408-409	41-42	14	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained,frameshift_variant	291-292	41-42	14	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1195793509,COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1195793509,COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1195793509,COSV99390761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=717;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained,frameshift_variant	294-295	41-42	14	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained,frameshift_variant	348-349	41-42	14	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained,frameshift_variant	291-292	41-42	14	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
634678	17:7676210-7676210	CATT	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,frameshift_variant,NMD_transcript_variant	301-302	41-42	14	W/*MX	tgg/tgAATGg	rs1195793509,COSV99390761	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	299-300	157-158	53	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	157-158	157-158	53	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	157-158	157-158	53	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	290-291	157-158	53	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	293-294	157-158	53	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	290-291	157-158	53	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	339-340	157-158	53	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	413-414	-	-	-	-	rs587782609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	295-296	157-158	53	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587782609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587782609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1092;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2624;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	296-297	157-158	53	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	407-408	40-41	14	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	290-291	40-41	14	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	293-294	40-41	14	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	347-348	40-41	14	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	290-291	40-41	14	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
142643	17:7676211-7676211	ATT	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	300-301	40-41	14	W/*W	tgg/tAATgg	rs587782609	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	300	158	53	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	158	158	53	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	158	158	53	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	291	158	53	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	294	158	53	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	291	158	53	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	340	158	53	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658483,COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658483,COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	414	-	-	-	-	rs876658483,COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	296	158	53	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876658483,COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658483,COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs876658483,COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658483,COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1092;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658483,COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2624;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	297	158	53	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	408	41	14	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	291	41	14	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658483,COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658483,COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658483,COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	294	41	14	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	348	41	14	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	291	41	14	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230285	17:7676211-7676211	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	301	41	14	W/*	tGg/tAg	rs876658483,COSV52774899	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	298-299	156-157	52-53	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	156-157	156-157	52-53	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	156-157	156-157	52-53	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	289-290	156-157	52-53	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	292-293	156-157	52-53	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	289-290	156-157	52-53	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	338-339	156-157	52-53	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=719;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=719;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	412-413	-	-	-	-	rs1555526748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	294-295	156-157	52-53	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=719;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1093;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2625;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	295-296	156-157	52-53	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	406-407	39-40	13-14	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	289-290	39-40	13-14	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=719;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=719;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=719;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	292-293	39-40	13-14	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	346-347	39-40	13-14	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	289-290	39-40	13-14	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
458525	17:7676212-7676212	T	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	299-300	39-40	13-14	-/X	-/A	rs1555526748	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	297-298	155-156	52	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	155-156	155-156	52	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	155-156	155-156	52	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	288-289	155-156	52	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	291-292	155-156	52	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	288-289	155-156	52	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	337-338	155-156	52	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526750	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526750	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	411-412	-	-	-	-	rs1555526750	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	293-294	155-156	52	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526750	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526750	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526750	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526750	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1094;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526750	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2626;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	294-295	155-156	52	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	405-406	38-39	13	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	288-289	38-39	13	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526750	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526750	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526750	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	291-292	38-39	13	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	345-346	38-39	13	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	288-289	38-39	13	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528265	17:7676212-7676214	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	298-299	38-39	13	Q/X	cAA/c	rs1555526750	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	296	154	52	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	154	154	52	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	154	154	52	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	287	154	52	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	290	154	52	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	287	154	52	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	336	154	52	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52734084,COSV53134595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52734084,COSV53134595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	410	-	-	-	-	COSV52734084,COSV53134595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	292	154	52	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52734084,COSV53134595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52734084,COSV53134595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52734084,COSV53134595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52734084,COSV53134595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1096;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52734084,COSV53134595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2628;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	293	154	52	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	404	37	13	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	287	37	13	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52734084,COSV53134595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52734084,COSV53134595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52734084,COSV53134595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	290	37	13	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	344	37	13	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	287	37	13	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1455400	17:7676215-7676215	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	297	37	13	Q/*	Caa/Taa	COSV52734084,COSV53134595	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	295-296	153-154	51-52	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	153-154	153-154	51-52	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	153-154	153-154	51-52	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	286-287	153-154	51-52	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	289-290	153-154	51-52	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	286-287	153-154	51-52	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	335-336	153-154	51-52	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556914,COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556914,COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	409-410	-	-	-	-	rs1567556914,COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	291-292	153-154	51-52	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567556914,COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556914,COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567556914,COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556914,COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1096;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556914,COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2628;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	292-293	153-154	51-52	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	403-404	36-37	12-13	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	286-287	36-37	12-13	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556914,COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556914,COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556914,COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	289-290	36-37	12-13	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	343-344	36-37	12-13	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	286-287	36-37	12-13	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634665	17:7676215-7676215	T	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	296-297	36-37	12-13	-/X	-/A	rs1567556914,COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	295-296	153-154	51-52	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	153-154	153-154	51-52	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	153-154	153-154	51-52	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	286-287	153-154	51-52	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	289-290	153-154	51-52	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	286-287	153-154	51-52	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	335-336	153-154	51-52	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	409-410	-	-	-	-	COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	291-292	153-154	51-52	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1096;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2628;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	292-293	153-154	51-52	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	403-404	36-37	12-13	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	286-287	36-37	12-13	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877599,COSV99400937	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	289-290	36-37	12-13	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	343-344	36-37	12-13	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	286-287	36-37	12-13	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
850480	17:7676215-7676215	TTCAATATCGTCCGGGGACAGCA	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	296-297	36-37	12-13	-/CCPRTILX	-/TGCTGTCCCCGGACGATATTGAA	COSV105877599,COSV99400937	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	294-295	152-153	51	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	152-153	152-153	51	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	152-153	152-153	51	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	285-286	152-153	51	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	288-289	152-153	51	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	285-286	152-153	51	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	334-335	152-153	51	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=723;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=723;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	408-409	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	290-291	152-153	51	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=723;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1097;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2629;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	291-292	152-153	51	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	402-403	35-36	12	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	285-286	35-36	12	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=723;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=723;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=723;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	288-289	35-36	12	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	342-343	35-36	12	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	285-286	35-36	12	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919200	17:7676216-7676216	TCAATATCGTC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	295-296	35-36	12	E/ETILX	gaa/gaGACGATATTGAa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	293	151	51	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	151	151	51	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	151	151	51	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	284	151	51	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	287	151	51	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	284	151	51	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	333	151	51	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556930,COSV52694020,COSV53536519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=725;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556930,COSV52694020,COSV53536519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=725;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	407	-	-	-	-	rs1567556930,COSV52694020,COSV53536519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	289	151	51	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567556930,COSV52694020,COSV53536519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556930,COSV52694020,COSV53536519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=725;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567556930,COSV52694020,COSV53536519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556930,COSV52694020,COSV53536519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1099;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556930,COSV52694020,COSV53536519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2631;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	290	151	51	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	401	34	12	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	284	34	12	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556930,COSV52694020,COSV53536519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=725;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556930,COSV52694020,COSV53536519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=725;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556930,COSV52694020,COSV53536519	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=725;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	287	34	12	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	341	34	12	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	284	34	12	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
568781	17:7676218-7676218	A	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	294	34	12	E/*	Gaa/Taa	rs1567556930,COSV52694020,COSV53536519	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	290-291	148-149	50	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	148-149	148-149	50	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	148-149	148-149	50	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	281-282	148-149	50	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	284-285	148-149	50	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	281-282	148-149	50	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	330-331	148-149	50	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556956,COSV104582708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=727;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556956,COSV104582708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=727;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	404-405	-	-	-	-	rs1567556956,COSV104582708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	286-287	148-149	50	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567556956,COSV104582708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556956,COSV104582708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=727;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567556956,COSV104582708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556956,COSV104582708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1101;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556956,COSV104582708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2633;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	287-288	148-149	50	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	398-399	31-32	11	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	281-282	31-32	11	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556956,COSV104582708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=727;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556956,COSV104582708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=727;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567556956,COSV104582708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=727;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	284-285	31-32	11	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	338-339	31-32	11	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	281-282	31-32	11	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1319403	17:7676220-7676220	T	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	291-292	31-32	11	I/NX	att/aAtt	rs1567556956,COSV104582708	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	282-283	140-141	47	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	140-141	140-141	47	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	140-141	140-141	47	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	273-274	140-141	47	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	276-277	140-141	47	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	273-274	140-141	47	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	322-323	140-141	47	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53080724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53080724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	396-397	-	-	-	-	COSV53080724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	278-279	140-141	47	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53080724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53080724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53080724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53080724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1109;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53080724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2641;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	279-280	140-141	47	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	390-391	23-24	8	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	273-274	23-24	8	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53080724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53080724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53080724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	276-277	23-24	8	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	330-331	23-24	8	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	273-274	23-24	8	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1771992	17:7676228-7676228	G	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	283-284	23-24	8	P/PX	ccg/ccCg	COSV53080724	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	282	140	47	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	140	140	47	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	140	140	47	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	273	140	47	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	276	140	47	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	273	140	47	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	322	140	47	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557016,COSV52838808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=736;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557016,COSV52838808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=736;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	396	-	-	-	-	rs1567557016,COSV52838808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	278	140	47	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567557016,COSV52838808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557016,COSV52838808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=736;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567557016,COSV52838808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557016,COSV52838808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1110;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557016,COSV52838808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2642;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	279	140	47	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	390	23	8	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	273	23	8	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557016,COSV52838808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=736;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557016,COSV52838808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=736;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557016,COSV52838808	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=736;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	276	23	8	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	330	23	8	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	273	23	8	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
574668	17:7676228-7676229	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	283	23	8	P/X	cCg/cg	rs1567557016,COSV52838808	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	279	137	46	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	137	137	46	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	137	137	46	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	270	137	46	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	273	137	46	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	270	137	46	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	319	137	46	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782650,COSV52729375,COSV52832767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=739;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782650,COSV52729375,COSV52832767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=739;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	393	-	-	-	-	rs587782650,COSV52729375,COSV52832767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	275	137	46	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587782650,COSV52729375,COSV52832767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782650,COSV52729375,COSV52832767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=739;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587782650,COSV52729375,COSV52832767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782650,COSV52729375,COSV52832767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1113;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782650,COSV52729375,COSV52832767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2645;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	276	137	46	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	387	20	7	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	270	20	7	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782650,COSV52729375,COSV52832767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=739;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782650,COSV52729375,COSV52832767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=739;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782650,COSV52729375,COSV52832767	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=739;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	273	20	7	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	327	20	7	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	270	20	7	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
142697	17:7676232-7676232	AC	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	280	20	7	S/CX	tCc/tGTc	rs587782650,COSV52729375,COSV52832767	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000269305.9	Transcript	inframe_deletion	266-274	124-132	42-44	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000359597.8	Transcript	inframe_deletion	124-132	124-132	42-44	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000413465.6	Transcript	inframe_deletion	124-132	124-132	42-44	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000420246.6	Transcript	inframe_deletion	257-265	124-132	42-44	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000445888.6	Transcript	inframe_deletion	260-268	124-132	42-44	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	257-265	124-132	42-44	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000503591.1	Transcript	inframe_deletion	306-314	124-132	42-44	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=744;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=744;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	380-388	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000508793.5	Transcript	inframe_deletion	262-270	124-132	42-44	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=744;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1118;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2650;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000604348.5	Transcript	inframe_deletion	263-271	124-132	42-44	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000610292.4	Transcript	inframe_deletion	374-382	7-15	3-5	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	257-265	7-15	3-5	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=744;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=744;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=744;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000619485.4	Transcript	inframe_deletion	260-268	7-15	3-5	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000620739.4	Transcript	inframe_deletion	314-322	7-15	3-5	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000622645.4	Transcript	inframe_deletion	257-265	7-15	3-5	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
986730	17:7676236-7676245	-	ENSG00000141510	ENST00000635293.1	Transcript	inframe_deletion,NMD_transcript_variant	267-275	7-15	3-5	DLM/-	GATTTGATG/-	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-271	?-129	?-43	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-129	?-129	?-43	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-129	?-129	?-43	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-262	?-129	?-43	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-265	?-129	?-43	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-262	?-129	?-43	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-311	?-129	?-43	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,non_coding_transcript_exon_variant,intron_variant	?-385	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-267	?-129	?-43	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1121;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2653;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,intron_variant	?-268	?-129	?-43	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant	?-379	?-12	?-4	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant	?-262	?-12	?-4	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant	?-265	?-12	?-4	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant	?-319	?-12	?-4	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant	?-262	?-12	?-4	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
998176	17:7676239-7676278	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,splice_polypyrimidine_tract_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant,NMD_transcript_variant	?-272	?-12	?-4	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	270	128	43	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	128	128	43	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	128	128	43	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	261	128	43	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	264	128	43	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	261	128	43	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	310	128	43	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	384	-	-	-	-	COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	266	128	43	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1122;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2654;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	267	128	43	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant	378	11	4	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant	261	11	4	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant	264	11	4	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant	318	11	4	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant	261	11	4	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
939637	17:7676240-7676241	-	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,NMD_transcript_variant	271	11	4	L/X	tTg/tg	COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained	270	128	43	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained	128	128	43	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained	128	128	43	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained	261	128	43	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained	264	128	43	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	261	128	43	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained	310	128	43	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526777,COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526777,COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	384	-	-	-	-	rs1555526777,COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained	266	128	43	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526777,COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526777,COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526777,COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526777,COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1122;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526777,COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2654;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained	267	128	43	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained	378	11	4	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	261	11	4	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526777,COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526777,COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526777,COSV52992944	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=748;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained	264	11	4	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained	318	11	4	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained	261	11	4	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
449749	17:7676241-7676241	T	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,NMD_transcript_variant	271	11	4	L/*	tTg/tAg	rs1555526777,COSV52992944	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	251-266	109-124	37-42	SQAMDD/X	TCCCAAGCAATGGATGat/at	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	109-124	109-124	37-42	SQAMDD/X	TCCCAAGCAATGGATGat/at	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	109-124	109-124	37-42	SQAMDD/X	TCCCAAGCAATGGATGat/at	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	242-257	109-124	37-42	SQAMDD/X	TCCCAAGCAATGGATGat/at	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	245-260	109-124	37-42	SQAMDD/X	TCCCAAGCAATGGATGat/at	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	242-257	109-124	37-42	SQAMDD/X	TCCCAAGCAATGGATGat/at	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	291-306	109-124	37-42	SQAMDD/X	TCCCAAGCAATGGATGat/at	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=752;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=752;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	365-380	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	247-262	109-124	37-42	SQAMDD/X	TCCCAAGCAATGGATGat/at	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=752;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1126;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2658;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	248-263	109-124	37-42	SQAMDD/X	TCCCAAGCAATGGATGat/at	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000610292.4	Transcript	start_lost,5_prime_UTR_variant	359-374	?-7	?-3	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000610538.4	Transcript	start_lost,5_prime_UTR_variant	242-257	?-7	?-3	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=752;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=752;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=752;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000619485.4	Transcript	start_lost,5_prime_UTR_variant	245-260	?-7	?-3	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000620739.4	Transcript	start_lost,5_prime_UTR_variant	299-314	?-7	?-3	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000622645.4	Transcript	start_lost,5_prime_UTR_variant	242-257	?-7	?-3	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1426924	17:7676244-7676260	-	ENSG00000141510	ENST00000635293.1	Transcript	start_lost,5_prime_UTR_variant,NMD_transcript_variant	252-267	?-7	?-3	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000269305.9	Transcript	stop_gained,frameshift_variant	266-267	124-125	42	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000359597.8	Transcript	stop_gained,frameshift_variant	124-125	124-125	42	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000413465.6	Transcript	stop_gained,frameshift_variant	124-125	124-125	42	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000420246.6	Transcript	stop_gained,frameshift_variant	257-258	124-125	42	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000445888.6	Transcript	stop_gained,frameshift_variant	260-261	124-125	42	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained,frameshift_variant	257-258	124-125	42	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000503591.1	Transcript	stop_gained,frameshift_variant	306-307	124-125	42	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=751;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=751;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	380-381	-	-	-	-	rs1555526784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000508793.5	Transcript	stop_gained,frameshift_variant	262-263	124-125	42	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=751;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1125;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2657;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000604348.5	Transcript	stop_gained,frameshift_variant	263-264	124-125	42	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000610292.4	Transcript	stop_gained,frameshift_variant	374-375	7-8	3	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained,frameshift_variant	257-258	7-8	3	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=751;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=751;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=751;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000619485.4	Transcript	stop_gained,frameshift_variant	260-261	7-8	3	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000620739.4	Transcript	stop_gained,frameshift_variant	314-315	7-8	3	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000622645.4	Transcript	stop_gained,frameshift_variant	257-258	7-8	3	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
480742	17:7676244-7676244	CATC	ENSG00000141510	ENST00000635293.1	Transcript	stop_gained,frameshift_variant,NMD_transcript_variant	267-268	7-8	3	D/G*X	gat/gGATGat	rs1555526784	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	261-262	119-120	40	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	119-120	119-120	40	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	119-120	119-120	40	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	252-253	119-120	40	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	255-256	119-120	40	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	252-253	119-120	40	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	301-302	119-120	40	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53289468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=756;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53289468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=756;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	375-376	-	-	-	-	COSV53289468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	257-258	119-120	40	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53289468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53289468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=756;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53289468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53289468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1130;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53289468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2662;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	258-259	119-120	40	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000610292.4	Transcript	frameshift_variant,start_lost	369-370	2-3	1	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant,start_lost	252-253	2-3	1	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53289468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=756;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53289468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=756;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53289468	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=756;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000619485.4	Transcript	frameshift_variant,start_lost	255-256	2-3	1	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000620739.4	Transcript	frameshift_variant,start_lost	309-310	2-3	1	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000622645.4	Transcript	frameshift_variant,start_lost	252-253	2-3	1	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1070793	17:7676249-7676249	A	ENSG00000141510	ENST00000635293.1	Transcript	frameshift_variant,start_lost,NMD_transcript_variant	262-263	2-3	1	M/IX	atg/atTg	COSV53289468	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	258-259	116-117	39	A/X	gCA/g	rs1555526793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	116-117	116-117	39	A/X	gCA/g	rs1555526793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	116-117	116-117	39	A/X	gCA/g	rs1555526793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	249-250	116-117	39	A/X	gCA/g	rs1555526793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	252-253	116-117	39	A/X	gCA/g	rs1555526793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	249-250	116-117	39	A/X	gCA/g	rs1555526793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	298-299	116-117	39	A/X	gCA/g	rs1555526793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	372-373	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	254-255	116-117	39	A/X	gCA/g	rs1555526793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1133;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2665;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	255-256	116-117	39	A/X	gCA/g	rs1555526793	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	366-367	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	249-250	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	252-253	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	306-307	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	249-250	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
492753	17:7676251-7676253	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	259-260	-	-	-	-	rs1555526793	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	254	112	38	Q/X	Caa/aa	rs1555526795,CM107390,COSV52689258	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	112	112	38	Q/X	Caa/aa	rs1555526795,CM107390,COSV52689258	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	112	112	38	Q/X	Caa/aa	rs1555526795,CM107390,COSV52689258	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	245	112	38	Q/X	Caa/aa	rs1555526795,CM107390,COSV52689258	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	248	112	38	Q/X	Caa/aa	rs1555526795,CM107390,COSV52689258	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	245	112	38	Q/X	Caa/aa	rs1555526795,CM107390,COSV52689258	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	294	112	38	Q/X	Caa/aa	rs1555526795,CM107390,COSV52689258	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=764;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=764;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	368	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	250	112	38	Q/X	Caa/aa	rs1555526795,CM107390,COSV52689258	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=764;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1138;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2670;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	251	112	38	Q/X	Caa/aa	rs1555526795,CM107390,COSV52689258	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	362	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	245	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=764;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=764;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=764;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	248	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	302	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	245	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
458519	17:7676256-7676257	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	255	-	-	-	-	rs1555526795,CM107390,COSV52689258	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	251	109	37	S/X	Tcc/cc	COSV53636396	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	109	109	37	S/X	Tcc/cc	COSV53636396	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	109	109	37	S/X	Tcc/cc	COSV53636396	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	242	109	37	S/X	Tcc/cc	COSV53636396	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	245	109	37	S/X	Tcc/cc	COSV53636396	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	242	109	37	S/X	Tcc/cc	COSV53636396	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	291	109	37	S/X	Tcc/cc	COSV53636396	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=767;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=767;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	365	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	247	109	37	S/X	Tcc/cc	COSV53636396	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=767;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1141;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2673;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	248	109	37	S/X	Tcc/cc	COSV53636396	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	359	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	242	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=767;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=767;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=767;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	245	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	299	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	242	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1713031	17:7676259-7676260	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	252	-	-	-	-	COSV53636396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	247	105	35	L/X	ttG/tt	COSV53067699,COSV53176324	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	105	105	35	L/X	ttG/tt	COSV53067699,COSV53176324	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	105	105	35	L/X	ttG/tt	COSV53067699,COSV53176324	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	238	105	35	L/X	ttG/tt	COSV53067699,COSV53176324	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	241	105	35	L/X	ttG/tt	COSV53067699,COSV53176324	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	238	105	35	L/X	ttG/tt	COSV53067699,COSV53176324	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	287	105	35	L/X	ttG/tt	COSV53067699,COSV53176324	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	361	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	243	105	35	L/X	ttG/tt	COSV53067699,COSV53176324	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1145;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2677;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	244	105	35	L/X	ttG/tt	COSV53067699,COSV53176324	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	355	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	238	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	241	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	295	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	238	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1779859	17:7676263-7676264	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	248	-	-	-	-	COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	246	104	35	L/X	tTg/tg	COSV52728232	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	104	104	35	L/X	tTg/tg	COSV52728232	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	104	104	35	L/X	tTg/tg	COSV52728232	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	237	104	35	L/X	tTg/tg	COSV52728232	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	240	104	35	L/X	tTg/tg	COSV52728232	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	237	104	35	L/X	tTg/tg	COSV52728232	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	286	104	35	L/X	tTg/tg	COSV52728232	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=772;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=772;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	360	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	242	104	35	L/X	tTg/tg	COSV52728232	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=772;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1146;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2678;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	243	104	35	L/X	tTg/tg	COSV52728232	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	354	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	237	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=772;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=772;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=772;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	240	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	294	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	237	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1776652	17:7676264-7676265	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	247	-	-	-	-	COSV52728232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	244	102	34	P/X	ccC/cc	COSV52833841	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	102	102	34	P/X	ccC/cc	COSV52833841	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	102	102	34	P/X	ccC/cc	COSV52833841	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	235	102	34	P/X	ccC/cc	COSV52833841	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	238	102	34	P/X	ccC/cc	COSV52833841	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	235	102	34	P/X	ccC/cc	COSV52833841	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	284	102	34	P/X	ccC/cc	COSV52833841	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	358	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	240	102	34	P/X	ccC/cc	COSV52833841	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1148;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2680;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	241	102	34	P/X	ccC/cc	COSV52833841	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	352	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	235	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	238	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	292	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	235	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1072141	17:7676266-7676267	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	245	-	-	-	-	COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	243-244	101-102	34	P/X	cCC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	101-102	101-102	34	P/X	cCC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	101-102	101-102	34	P/X	cCC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	234-235	101-102	34	P/X	cCC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	237-238	101-102	34	P/X	cCC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	234-235	101-102	34	P/X	cCC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	283-284	101-102	34	P/X	cCC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	357-358	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	239-240	101-102	34	P/X	cCC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1148;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2680;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	240-241	101-102	34	P/X	cCC/c	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	351-352	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	234-235	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	237-238	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	291-292	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	234-235	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1798624	17:7676266-7676268	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	244-245	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	244-245	102-103	34-35	-/X	-/C	COSV52674838	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	102-103	102-103	34-35	-/X	-/C	COSV52674838	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	102-103	102-103	34-35	-/X	-/C	COSV52674838	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	235-236	102-103	34-35	-/X	-/C	COSV52674838	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	238-239	102-103	34-35	-/X	-/C	COSV52674838	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	235-236	102-103	34-35	-/X	-/C	COSV52674838	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	284-285	102-103	34-35	-/X	-/C	COSV52674838	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=773;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=773;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	358-359	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	240-241	102-103	34-35	-/X	-/C	COSV52674838	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=773;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1147;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2679;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	241-242	102-103	34-35	-/X	-/C	COSV52674838	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	352-353	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	235-236	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=773;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=773;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=773;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	238-239	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	292-293	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	235-236	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
960090	17:7676266-7676266	G	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	245-246	-	-	-	-	COSV52674838	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant,splice_region_variant	239-240	97-98	33	S/FX	tcc/tTcc	rs1131691041,COSV52680743,COSV99383879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant,splice_region_variant	97-98	97-98	33	S/FX	tcc/tTcc	rs1131691041,COSV52680743,COSV99383879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant,splice_region_variant	97-98	97-98	33	S/FX	tcc/tTcc	rs1131691041,COSV52680743,COSV99383879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant,splice_region_variant	230-231	97-98	33	S/FX	tcc/tTcc	rs1131691041,COSV52680743,COSV99383879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant,splice_region_variant	233-234	97-98	33	S/FX	tcc/tTcc	rs1131691041,COSV52680743,COSV99383879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant,splice_region_variant	230-231	97-98	33	S/FX	tcc/tTcc	rs1131691041,COSV52680743,COSV99383879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant,splice_region_variant	279-280	97-98	33	S/FX	tcc/tTcc	rs1131691041,COSV52680743,COSV99383879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=778;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=778;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	353-354	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant,splice_region_variant	235-236	97-98	33	S/FX	tcc/tTcc	rs1131691041,COSV52680743,COSV99383879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=778;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1152;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2684;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant,splice_region_variant	236-237	97-98	33	S/FX	tcc/tTcc	rs1131691041,COSV52680743,COSV99383879	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,5_prime_UTR_variant	347-348	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,5_prime_UTR_variant	230-231	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=778;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=778;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=778;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,5_prime_UTR_variant	233-234	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,5_prime_UTR_variant	287-288	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,5_prime_UTR_variant	230-231	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
428907	17:7676271-7676271	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,5_prime_UTR_variant,NMD_transcript_variant	240-241	-	-	-	-	rs1131691041,COSV52680743,COSV99383879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1;PHENO=1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=781;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=781;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=781;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1155;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2687;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=781;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=781;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=781;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
634786	17:7676273-7676274	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs1567557258,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=780;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=780;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=780;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1154;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2686;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=780;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=780;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=780;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
638853	17:7676273-7676273	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic,not_provided;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=780;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=780;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=780;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1154;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2686;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=780;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=780;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=780;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
656497	17:7676273-7676273	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs1597375294,CS971912,COSV52665806,COSV52762622,COSV52838014	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=781;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=781;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_acceptor_variant,non_coding_transcript_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=781;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1155;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2687;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=781;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=781;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=781;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
246337	17:7676274-7676274	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs879254212,COSV52678373,COSV52848662,COSV53375861,COSV53887648	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=790;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=790;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=790;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1164;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2696;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=790;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=790;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=790;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
638852	17:7676283-7676283	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1;PHENO=1,1,1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant,splice_donor_region_variant,coding_sequence_variant,intron_variant	228-?	86-?	29-?	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant,splice_donor_region_variant,coding_sequence_variant,intron_variant	86-?	86-?	29-?	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant,splice_donor_region_variant,coding_sequence_variant,intron_variant	86-?	86-?	29-?	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,splice_donor_region_variant,coding_sequence_variant,intron_variant	219-?	86-?	29-?	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant,splice_donor_region_variant,coding_sequence_variant,intron_variant	222-?	86-?	29-?	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,splice_donor_region_variant,coding_sequence_variant,intron_variant	219-?	86-?	29-?	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant,splice_donor_region_variant,coding_sequence_variant,intron_variant	268-?	86-?	29-?	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526916	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=885;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526916	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=885;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,splice_donor_region_variant,non_coding_transcript_exon_variant,intron_variant	342-?	-	-	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant,splice_donor_region_variant,coding_sequence_variant,intron_variant	224-?	86-?	29-?	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526916	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526916	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=885;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant,splice_donor_region_variant,coding_sequence_variant,intron_variant	165-?	86-?	29-?	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526916	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1259;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526916	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2791;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant,splice_donor_region_variant,coding_sequence_variant,intron_variant	225-?	86-?	29-?	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant,splice_donor_region_variant,5_prime_UTR_variant,intron_variant	336-?	-	-	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,splice_donor_region_variant,5_prime_UTR_variant,intron_variant	219-?	-	-	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526916	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=885;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526916	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=885;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526916	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=885;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant,splice_donor_region_variant,5_prime_UTR_variant,intron_variant	222-?	-	-	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant,splice_donor_region_variant,5_prime_UTR_variant,intron_variant	276-?	-	-	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,splice_donor_region_variant,5_prime_UTR_variant,intron_variant	219-?	-	-	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428881	17:7676377-7676392	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,splice_donor_region_variant,5_prime_UTR_variant,intron_variant,NMD_transcript_variant	229-?	-	-	-	-	rs1555526916	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=886;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=886;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1131691015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=886;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1260;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2792;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=886;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=886;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691015	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=886;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
428875	17:7676379-7676379	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1131691015	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1262;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2794;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1067373	17:7676380-7676381	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1261;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2793;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1467852	17:7676380-7676380	CCAGAACGTT	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1261;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2793;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=887;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
948068	17:7676380-7676380	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs2073505429,COSV53738354	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1262;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2794;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
428859	17:7676381-7676381	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1262;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2794;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482212	17:7676381-7676381	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	rs1131691003,CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000503591.1	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_donor_variant,non_coding_transcript_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000508793.5	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1262;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2794;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
860797	17:7676381-7676381	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_variant,NMD_transcript_variant	-	-	-	-	-	CS167193,COSV52662718,COSV52757202,COSV53162510	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant,splice_region_variant	237	95	32	L/X	cTg/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant,splice_region_variant	95	95	32	L/X	cTg/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant,splice_region_variant	95	95	32	L/X	cTg/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant,splice_region_variant	228	95	32	L/X	cTg/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant,splice_region_variant	231	95	32	L/X	cTg/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant,splice_region_variant	228	95	32	L/X	cTg/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant,splice_region_variant	277	95	32	L/X	cTg/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=890;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=890;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	351	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant,splice_region_variant	233	95	32	L/X	cTg/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=890;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant,splice_region_variant	174	95	32	L/X	cTg/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1264;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2796;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant,splice_region_variant	234	95	32	L/X	cTg/cg	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,5_prime_UTR_variant	345	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,5_prime_UTR_variant	228	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=890;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=890;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=890;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,5_prime_UTR_variant	231	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,5_prime_UTR_variant	285	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,5_prime_UTR_variant	228	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767527	17:7676382-7676383	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,5_prime_UTR_variant,NMD_transcript_variant	238	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	235	93	31	V/X	gtT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	93	93	31	V/X	gtT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	93	93	31	V/X	gtT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	226	93	31	V/X	gtT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	229	93	31	V/X	gtT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	226	93	31	V/X	gtT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	275	93	31	V/X	gtT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	349	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	231	93	31	V/X	gtT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	172	93	31	V/X	gtT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1266;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2798;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	232	93	31	V/X	gtT/gt	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	343	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	226	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	229	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	283	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	226	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1075116	17:7676384-7676385	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	236	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	232	90	30	N/X	aaC/aa	COSV53166880,COSV99396148	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	90	90	30	N/X	aaC/aa	COSV53166880,COSV99396148	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	90	90	30	N/X	aaC/aa	COSV53166880,COSV99396148	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	223	90	30	N/X	aaC/aa	COSV53166880,COSV99396148	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	226	90	30	N/X	aaC/aa	COSV53166880,COSV99396148	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	223	90	30	N/X	aaC/aa	COSV53166880,COSV99396148	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	272	90	30	N/X	aaC/aa	COSV53166880,COSV99396148	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	346	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	228	90	30	N/X	aaC/aa	COSV53166880,COSV99396148	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	169	90	30	N/X	aaC/aa	COSV53166880,COSV99396148	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1269;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2801;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	229	90	30	N/X	aaC/aa	COSV53166880,COSV99396148	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	340	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	223	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	226	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	280	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	223	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765799	17:7676387-7676388	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	233	-	-	-	-	COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	232-233	90-91	30-31	-/X	-/A	rs1131691618,COSV105016597	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	90-91	90-91	30-31	-/X	-/A	rs1131691618,COSV105016597	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	90-91	90-91	30-31	-/X	-/A	rs1131691618,COSV105016597	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	223-224	90-91	30-31	-/X	-/A	rs1131691618,COSV105016597	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	226-227	90-91	30-31	-/X	-/A	rs1131691618,COSV105016597	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	223-224	90-91	30-31	-/X	-/A	rs1131691618,COSV105016597	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	272-273	90-91	30-31	-/X	-/A	rs1131691618,COSV105016597	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=894;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=894;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	346-347	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	228-229	90-91	30-31	-/X	-/A	rs1131691618,COSV105016597	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=894;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	169-170	90-91	30-31	-/X	-/A	rs1131691618,COSV105016597	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1268;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2800;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	229-230	90-91	30-31	-/X	-/A	rs1131691618,COSV105016597	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	340-341	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	223-224	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=894;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=894;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=894;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	226-227	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	280-281	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	223-224	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
429829	17:7676387-7676387	T	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	233-234	-	-	-	-	rs1131691618,COSV105016597	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	231	89	30	N/X	aAc/ac	COSV105025587	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	89	89	30	N/X	aAc/ac	COSV105025587	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	89	89	30	N/X	aAc/ac	COSV105025587	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	222	89	30	N/X	aAc/ac	COSV105025587	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	225	89	30	N/X	aAc/ac	COSV105025587	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	222	89	30	N/X	aAc/ac	COSV105025587	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	271	89	30	N/X	aAc/ac	COSV105025587	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=896;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=896;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	345	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	227	89	30	N/X	aAc/ac	COSV105025587	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=896;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	168	89	30	N/X	aAc/ac	COSV105025587	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1270;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2802;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	228	89	30	N/X	aAc/ac	COSV105025587	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	339	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	222	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=896;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=896;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=896;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	225	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	279	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	222	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1765403	17:7676388-7676389	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	232	-	-	-	-	COSV105025587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	228	86	29	N/X	aAc/ac	rs1555526931	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	86	86	29	N/X	aAc/ac	rs1555526931	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	86	86	29	N/X	aAc/ac	rs1555526931	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	219	86	29	N/X	aAc/ac	rs1555526931	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	222	86	29	N/X	aAc/ac	rs1555526931	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	219	86	29	N/X	aAc/ac	rs1555526931	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	268	86	29	N/X	aAc/ac	rs1555526931	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=899;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=899;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	342	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	224	86	29	N/X	aAc/ac	rs1555526931	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=899;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	165	86	29	N/X	aAc/ac	rs1555526931	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1273;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2805;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	225	86	29	N/X	aAc/ac	rs1555526931	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	336	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	219	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=899;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=899;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=899;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	222	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	276	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	219	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528243	17:7676391-7676392	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	229	-	-	-	-	rs1555526931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	222	80	27	P/X	cCt/ct	rs1192416464,COSV53662521	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	80	80	27	P/X	cCt/ct	rs1192416464,COSV53662521	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	80	80	27	P/X	cCt/ct	rs1192416464,COSV53662521	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	213	80	27	P/X	cCt/ct	rs1192416464,COSV53662521	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	216	80	27	P/X	cCt/ct	rs1192416464,COSV53662521	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	213	80	27	P/X	cCt/ct	rs1192416464,COSV53662521	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	262	80	27	P/X	cCt/ct	rs1192416464,COSV53662521	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	336	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	218	80	27	P/X	cCt/ct	rs1192416464,COSV53662521	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	159	80	27	P/X	cCt/ct	rs1192416464,COSV53662521	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1279;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2811;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	219	80	27	P/X	cCt/ct	rs1192416464,COSV53662521	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	330	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	213	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	216	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	270	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	213	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
1447671	17:7676397-7676398	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	223	-	-	-	-	rs1192416464,COSV53662521	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant,frameshift_variant	219-222	77-80	26-27	LP/QERX	cTTCCt/cAAGAACGTt	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant,frameshift_variant	77-80	77-80	26-27	LP/QERX	cTTCCt/cAAGAACGTt	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant,frameshift_variant	77-80	77-80	26-27	LP/QERX	cTTCCt/cAAGAACGTt	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant,frameshift_variant	210-213	77-80	26-27	LP/QERX	cTTCCt/cAAGAACGTt	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant,frameshift_variant	213-216	77-80	26-27	LP/QERX	cTTCCt/cAAGAACGTt	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant,frameshift_variant	210-213	77-80	26-27	LP/QERX	cTTCCt/cAAGAACGTt	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant,frameshift_variant	259-262	77-80	26-27	LP/QERX	cTTCCt/cAAGAACGTt	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs397516438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs397516438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	333-336	-	-	-	-	rs397516438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant,frameshift_variant	215-218	77-80	26-27	LP/QERX	cTTCCt/cAAGAACGTt	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs397516438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs397516438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant,frameshift_variant	156-159	77-80	26-27	LP/QERX	cTTCCt/cAAGAACGTt	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs397516438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1279;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs397516438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2811;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant,frameshift_variant	216-219	77-80	26-27	LP/QERX	cTTCCt/cAAGAACGTt	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	327-330	-	-	-	-	rs397516438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant,5_prime_UTR_variant	210-213	-	-	-	-	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs397516438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs397516438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs397516438	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant,5_prime_UTR_variant	213-216	-	-	-	-	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant,5_prime_UTR_variant	267-270	-	-	-	-	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant,5_prime_UTR_variant	210-213	-	-	-	-	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,5_prime_UTR_variant,NMD_transcript_variant	220-223	-	-	-	-	rs397516438	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
43593	17:7676398-7676401	ACGTTCTT	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs397516438	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=pathogenic,likely_pathogenic;PHENO=1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=911;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=911;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	330	-	-	-	-	COSV53294543,COSV99037345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=911;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1285;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2817;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	324	-	-	-	-	COSV53294543,COSV99037345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=911;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=911;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=911;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1068266	17:7676404-7676404	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV53294543,COSV99037345	IMPACT=MODIFIER;BIOTYPE=enhancer;SOMATIC=1,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=912;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=912;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	329	-	-	-	-	rs1131691020,COSV99463573	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=912;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1286;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2818;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000604348.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	323	-	-	-	-	rs1131691020,COSV99463573	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=912;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=912;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=912;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_acceptor_variant,NMD_transcript_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
428882	17:7676405-7676405	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1131691020,COSV99463573	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=not_provided,likely_pathogenic;SOMATIC=0,1;PHENO=1,1
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant,splice_region_variant	214-215	72-73	24-25	-/X	-/A	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant,splice_region_variant	72-73	72-73	24-25	-/X	-/A	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant,splice_region_variant	72-73	72-73	24-25	-/X	-/A	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant,splice_region_variant	205-206	72-73	24-25	-/X	-/A	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant,splice_region_variant	208-209	72-73	24-25	-/X	-/A	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant,splice_region_variant	205-206	72-73	24-25	-/X	-/A	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant,splice_region_variant	254-255	72-73	24-25	-/X	-/A	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1029;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1029;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	211-212	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant,splice_region_variant	210-211	72-73	24-25	-/X	-/A	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1029;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant,splice_region_variant	151-152	72-73	24-25	-/X	-/A	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1403;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2935;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant,splice_region_variant	211-212	72-73	24-25	-/X	-/A	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	205-206	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,5_prime_UTR_variant	205-206	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1029;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1029;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1029;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,5_prime_UTR_variant	208-209	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,5_prime_UTR_variant	262-263	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,5_prime_UTR_variant	205-206	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,5_prime_UTR_variant,NMD_transcript_variant	215-216	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1341341	17:7676522-7676522	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=enhancer
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant,splice_region_variant	214	72	24	K/X	aaA/aa	CD137623	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant,splice_region_variant	72	72	24	K/X	aaA/aa	CD137623	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant,splice_region_variant	72	72	24	K/X	aaA/aa	CD137623	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant,splice_region_variant	205	72	24	K/X	aaA/aa	CD137623	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant,splice_region_variant	208	72	24	K/X	aaA/aa	CD137623	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant,splice_region_variant	205	72	24	K/X	aaA/aa	CD137623	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant,splice_region_variant	254	72	24	K/X	aaA/aa	CD137623	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	211	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant,splice_region_variant	210	72	24	K/X	aaA/aa	CD137623	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant,splice_region_variant	151	72	24	K/X	aaA/aa	CD137623	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1404;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2936;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant,splice_region_variant	211	72	24	K/X	aaA/aa	CD137623	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	205	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,5_prime_UTR_variant	205	-	-	-	-	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,5_prime_UTR_variant	208	-	-	-	-	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,5_prime_UTR_variant	262	-	-	-	-	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,5_prime_UTR_variant	205	-	-	-	-	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,5_prime_UTR_variant,NMD_transcript_variant	215	-	-	-	-	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1458385	17:7676522-7676523	-	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;BIOTYPE=enhancer;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	200	58	20	S/X	Tca/ca	rs1131691018	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	58	58	20	S/X	Tca/ca	rs1131691018	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	58	58	20	S/X	Tca/ca	rs1131691018	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	191	58	20	S/X	Tca/ca	rs1131691018	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	194	58	20	S/X	Tca/ca	rs1131691018	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	191	58	20	S/X	Tca/ca	rs1131691018	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	240	58	20	S/X	Tca/ca	rs1131691018	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1044;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1044;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	197	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	196	58	20	S/X	Tca/ca	rs1131691018	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1044;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	137	58	20	S/X	Tca/ca	rs1131691018	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1418;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2950;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	197	58	20	S/X	Tca/ca	rs1131691018	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	191	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	191	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1044;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1044;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1044;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	194	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	248	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	191	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	201	-	-	-	-	rs1131691018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
428880	17:7676536-7676537	-	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1131691018	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=pathogenic;PHENO=1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	194	52	18	T/X	Aca/ca	rs876658627,COSV53626375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	52	52	18	T/X	Aca/ca	rs876658627,COSV53626375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	52	52	18	T/X	Aca/ca	rs876658627,COSV53626375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	185	52	18	T/X	Aca/ca	rs876658627,COSV53626375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	188	52	18	T/X	Aca/ca	rs876658627,COSV53626375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	185	52	18	T/X	Aca/ca	rs876658627,COSV53626375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	234	52	18	T/X	Aca/ca	rs876658627,COSV53626375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1050;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1050;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	191	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	190	52	18	T/X	Aca/ca	rs876658627,COSV53626375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1050;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	131	52	18	T/X	Aca/ca	rs876658627,COSV53626375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1424;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2956;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	191	52	18	T/X	Aca/ca	rs876658627,COSV53626375	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	185	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	185	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1050;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1050;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1050;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	188	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	242	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	185	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	195	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
230550	17:7676542-7676543	-	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs876658627,COSV53626375	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=pathogenic;SOMATIC=0,1;PHENO=1,1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	187	45	15	S/X	agT/ag	rs1555526997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	45	45	15	S/X	agT/ag	rs1555526997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	45	45	15	S/X	agT/ag	rs1555526997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	178	45	15	S/X	agT/ag	rs1555526997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	181	45	15	S/X	agT/ag	rs1555526997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	178	45	15	S/X	agT/ag	rs1555526997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	227	45	15	S/X	agT/ag	rs1555526997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	184	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	183	45	15	S/X	agT/ag	rs1555526997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	124	45	15	S/X	agT/ag	rs1555526997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1431;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2963;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	184	45	15	S/X	agT/ag	rs1555526997	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	178	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	178	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	181	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	235	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	178	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	188	-	-	-	-	rs1555526997	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=pathogenic;PHENO=1
528242	17:7676549-7676550	-	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555526997	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000269305.9	Transcript	frameshift_variant	180-181	38-39	13	P/PX	cct/ccCt	rs1555527002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000359597.8	Transcript	frameshift_variant	38-39	38-39	13	P/PX	cct/ccCt	rs1555527002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000413465.6	Transcript	frameshift_variant	38-39	38-39	13	P/PX	cct/ccCt	rs1555527002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000420246.6	Transcript	frameshift_variant	171-172	38-39	13	P/PX	cct/ccCt	rs1555527002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000445888.6	Transcript	frameshift_variant	174-175	38-39	13	P/PX	cct/ccCt	rs1555527002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant	171-172	38-39	13	P/PX	cct/ccCt	rs1555527002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000503591.1	Transcript	frameshift_variant	220-221	38-39	13	P/PX	cct/ccCt	rs1555527002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1063;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1063;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	177-178	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000508793.5	Transcript	frameshift_variant	176-177	38-39	13	P/PX	cct/ccCt	rs1555527002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1063;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000514944.5	Transcript	frameshift_variant	117-118	38-39	13	P/PX	cct/ccCt	rs1555527002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1437;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2969;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000604348.5	Transcript	frameshift_variant	177-178	38-39	13	P/PX	cct/ccCt	rs1555527002	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	171-172	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	171-172	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1063;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1063;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1063;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	174-175	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	228-229	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	171-172	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	181-182	-	-	-	-	rs1555527002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_pathogenic;PHENO=1
487431	17:7676556-7676556	G	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555527002	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_pathogenic;PHENO=1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1278	1136	379	R/H	cGc/cAc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1402	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1272	1136	379	R/H	cGc/cAc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1329	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1078	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1018	740	247	R/H	cGc/cAc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4871;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3880;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1151	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4562;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000576024.1	Transcript	synonymous_variant	89	90	30	P	ccG/ccA	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1386	1019	340	R/H	cGc/cAc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1329	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1078	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1151	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1018	659	220	R/H	cGc/cAc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1272	1019	340	R/H	cGc/cAc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1326	1019	340	R/H	cGc/cAc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1402	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
246221	17:7669655-7669655	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1238	1096	366	S/A	Tcc/Gcc	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1362	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1232	1096	366	S/A	Tcc/Gcc	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1289	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4616;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1038	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	978	700	234	S/A	Tcc/Gcc	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3913;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4503;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2922;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1111	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3604;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3641;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4549;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1346	979	327	S/A	Tcc/Gcc	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1289	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1038	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1111	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	978	619	207	S/A	Tcc/Gcc	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1232	979	327	S/A	Tcc/Gcc	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1286	979	327	S/A	Tcc/Gcc	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1362	-	-	-	-	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
135360	17:7670613-7670613	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1239	979	327	S/A	Tcc/Gcc	rs17881470,CM078492,COSV106055876,COSV52875421	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1235	1093	365	H/Y	Cac/Tac	rs267605075,CM031388,COSV53001057	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1359	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1229	1093	365	H/Y	Cac/Tac	rs267605075,CM031388,COSV53001057	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1286	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4613;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1035	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	975	697	233	H/Y	Cac/Tac	rs267605075,CM031388,COSV53001057	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3910;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4500;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2919;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1108	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3601;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3638;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4546;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1343	976	326	H/Y	Cac/Tac	rs267605075,CM031388,COSV53001057	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1286	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1035	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1108	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	975	616	206	H/Y	Cac/Tac	rs267605075,CM031388,COSV53001057	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1229	976	326	H/Y	Cac/Tac	rs267605075,CM031388,COSV53001057	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1283	976	326	H/Y	Cac/Tac	rs267605075,CM031388,COSV53001057	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1359	-	-	-	-	rs267605075,CM031388,COSV53001057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
80708	17:7670616-7670616	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1236	976	326	H/Y	Cac/Tac	rs267605075,CM031388,COSV53001057	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1221	1079	360	G/A	gGg/gCg	rs35993958,CM035962,COSV52666301	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1345	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1215	1079	360	G/A	gGg/gCg	rs35993958,CM035962,COSV52666301	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1272	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4599;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1021	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	961	683	228	G/A	gGg/gCg	rs35993958,CM035962,COSV52666301	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3896;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4486;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2905;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1094	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3587;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3624;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4532;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1329	962	321	G/A	gGg/gCg	rs35993958,CM035962,COSV52666301	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1272	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1021	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1094	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	961	602	201	G/A	gGg/gCg	rs35993958,CM035962,COSV52666301	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1215	962	321	G/A	gGg/gCg	rs35993958,CM035962,COSV52666301	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1269	962	321	G/A	gGg/gCg	rs35993958,CM035962,COSV52666301	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1345	-	-	-	-	rs35993958,CM035962,COSV52666301	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
142003	17:7670630-7670630	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1222	962	321	G/A	gGg/gCg	rs35993958,CM035962,COSV52666301	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1202	1060	354	Q/K	Cag/Aag	rs755394212,COSV52783779,COSV53018657	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1326	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1196	1060	354	Q/K	Cag/Aag	rs755394212,COSV52783779,COSV53018657	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1253	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4580;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1002	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	942	664	222	Q/K	Cag/Aag	rs755394212,COSV52783779,COSV53018657	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3877;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4467;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2886;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1075	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3568;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3605;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4513;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1310	943	315	Q/K	Cag/Aag	rs755394212,COSV52783779,COSV53018657	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1253	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1002	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1075	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	942	583	195	Q/K	Cag/Aag	rs755394212,COSV52783779,COSV53018657	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1196	943	315	Q/K	Cag/Aag	rs755394212,COSV52783779,COSV53018657	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1250	943	315	Q/K	Cag/Aag	rs755394212,COSV52783779,COSV53018657	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1326	-	-	-	-	rs755394212,COSV52783779,COSV53018657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231485	17:7670649-7670649	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1203	943	315	Q/K	Cag/Aag	rs755394212,COSV52783779,COSV53018657	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1167	1025	342	R/Q	cGa/cAa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1291	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1161	1025	342	R/Q	cGa/cAa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1218	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4545;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	967	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	907	629	210	R/Q	cGa/cAa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3842;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4432;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2851;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1040	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3533;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3570;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4478;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1275	908	303	R/Q	cGa/cAa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1218	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	967	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1040	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	907	548	183	R/Q	cGa/cAa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1161	908	303	R/Q	cGa/cAa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1215	908	303	R/Q	cGa/cAa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1291	-	-	-	-	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233136	17:7670684-7670684	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1168	908	303	R/Q	cGa/cAa	rs375338359,CM098494,COSV52690857,COSV52980226,COSV53438718	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1157	1015	339	E/Q	Gag/Cag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1281	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1151	1015	339	E/Q	Gag/Cag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1208	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4535;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	957	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	897	619	207	E/Q	Gag/Cag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4422;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2841;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1030	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3523;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3560;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4468;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1265	898	300	E/Q	Gag/Cag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1208	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	957	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1030	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	897	538	180	E/Q	Gag/Cag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1151	898	300	E/Q	Gag/Cag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1205	898	300	E/Q	Gag/Cag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1281	-	-	-	-	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141893	17:7670694-7670694	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1158	898	300	E/Q	Gag/Cag	rs17882252,CM984588,COSV52705645,COSV52980241,COSV53040770,COSV53664260	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1091	949	317	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	949	949	317	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1082	949	317	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1085	949	317	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1082	949	317	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1650;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	831	553	185	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	831	553	185	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=947;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1537;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	685	553	185	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	831	553	185	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=638;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=675;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant	9	10	4	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1583;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1199	832	278	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1082	832	278	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	831	472	158	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	831	472	158	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	831	472	158	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1085	832	278	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1139	832	278	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1082	832	278	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1092	832	278	Q/K	Cag/Aag	rs764735889,COSV52685086,COSV53209009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231008	17:7673579-7673579	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs764735889,COSV52685086,COSV53209009	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1077	935	312	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	935	935	312	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1068	935	312	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1071	935	312	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1068	935	312	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1636;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	817	539	180	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	817	539	180	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=933;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1523;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	671	539	180	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	817	539	180	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=624;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=6;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1569;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1185	818	273	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1068	818	273	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	817	458	153	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	817	458	153	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	817	458	153	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1071	818	273	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1125	818	273	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1068	818	273	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1078	818	273	T/S	aCc/aGc	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141102	17:7673593-7673593	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs145151284,CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=benign,uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1034	892	298	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	892	892	298	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1025	892	298	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1028	892	298	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1025	892	298	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1501;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	774	496	166	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	774	496	166	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=798;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1388;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	628	496	166	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	774	496	166	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=489;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=526;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=141;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1434;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1142	775	259	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1025	775	259	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	774	415	139	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	774	415	139	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	774	415	139	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1028	775	259	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1082	775	259	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1025	775	259	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1035	775	259	E/K	Gag/Aag	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
141483	17:7673728-7673728	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs201744589,CM031387,COSV52661551,COSV52761493,COSV53353479,COSV53790595	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1028	886	296	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	886	886	296	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1019	886	296	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1022	886	296	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1019	886	296	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1495;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	768	490	164	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	768	490	164	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=792;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1382;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	622	490	164	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	768	490	164	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=483;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=520;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=147;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1428;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1136	769	257	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1019	769	257	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	768	409	137	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	768	409	137	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	768	409	137	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1022	769	257	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1076	769	257	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1019	769	257	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1029	769	257	H/Y	Cac/Tac	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132973	17:7673734-7673734	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs672601296,COSV52949796,COSV52994463,COSV53210146	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1019	877	293	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	877	877	293	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1010	877	293	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1013	877	293	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1010	877	293	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1486;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	759	481	161	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	759	481	161	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=783;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1373;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	613	481	161	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	759	481	161	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=474;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=511;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=156;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1419;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1127	760	254	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1010	760	254	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	759	400	134	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	759	400	134	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	759	400	134	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1013	760	254	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1067	760	254	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1010	760	254	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1020	760	254	G/W	Ggg/Tgg	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127826	17:7673743-7673743	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs587780076,CM910627,COSV52684774,COSV52689066,COSV52730603,COSV52752246	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1011	869	290	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	869	869	290	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1002	869	290	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1005	869	290	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1002	869	290	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1478;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	751	473	158	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	751	473	158	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=775;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1365;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	605	473	158	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	751	473	158	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=466;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=503;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=164;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1411;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1119	752	251	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1002	752	251	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	751	392	131	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	751	392	131	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	751	392	131	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1005	752	251	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1059	752	251	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1002	752	251	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1012	752	251	R/H	cGc/cAc	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
127825	17:7673751-7673751	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs55819519,CM065493,CM993905,COSV52683585,COSV53296796	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance,benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1010	868	290	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	868	868	290	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs770374782,COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1001	868	290	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1004	868	290	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1001	868	290	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs770374782,COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1477;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	750	472	158	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	750	472	158	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs770374782,COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs770374782,COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1364;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	604	472	158	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	750	472	158	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs770374782,COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=465;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs770374782,COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=502;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs770374782,COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=165;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs770374782,COSV52761356,COSV53509681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1410;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1118	751	251	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1001	751	251	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	750	391	131	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	750	391	131	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	750	391	131	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1004	751	251	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1058	751	251	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1001	751	251	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1011	751	251	R/C	Cgc/Tgc	rs770374782,COSV52761356,COSV53509681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216472	17:7673752-7673752	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs770374782,COSV52761356,COSV53509681	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	993	851	284	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	851	851	284	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs863224685,CD003107,COSV52908002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	984	851	284	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	987	851	284	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	984	851	284	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224685,CD003107,COSV52908002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1460;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	733	455	152	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	733	455	152	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224685,CD003107,COSV52908002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=757;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224685,CD003107,COSV52908002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1347;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	587	455	152	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	733	455	152	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224685,CD003107,COSV52908002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=448;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224685,CD003107,COSV52908002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=485;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs863224685,CD003107,COSV52908002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=182;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224685,CD003107,COSV52908002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1393;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1101	734	245	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	984	734	245	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	733	374	125	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	733	374	125	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	733	374	125	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	987	734	245	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1041	734	245	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	984	734	245	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	994	734	245	T/I	aCa/aTa	rs863224685,CD003107,COSV52908002	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
216471	17:7673769-7673769	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs863224685,CD003107,COSV52908002	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	989	847	283	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	847	847	283	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	980	847	283	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	983	847	283	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	980	847	283	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1456;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	729	451	151	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	729	451	151	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=753;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1343;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	583	451	151	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	729	451	151	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=444;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=481;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=186;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1389;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1097	730	244	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	980	730	244	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	729	370	124	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	729	370	124	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	729	370	124	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	983	730	244	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1037	730	244	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	980	730	244	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	990	730	244	R/C	Cgc/Tgc	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127824	17:7673773-7673773	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs149633775,CM041458,COSV52676681,COSV52751436,COSV52937605,COSV53235263	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance,likely_benign,likely_pathogenic,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	921	779	260	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	779	779	260	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	779	779	260	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	912	779	260	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	915	779	260	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	912	779	260	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1045;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	661	383	128	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	661	383	128	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=342;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=932;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	515	383	128	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	661	383	128	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=33;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=70;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=978;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1029	662	221	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	912	662	221	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	661	302	101	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	661	302	101	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	661	302	101	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	915	662	221	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	969	662	221	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	912	662	221	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
231033	17:7674184-7674184	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	922	662	221	S/Y	tCc/tAc	rs876658916,COSV52661443,COSV52698464,COSV52760769,COSV52978505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	846	704	235	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	704	704	235	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	704	704	235	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	837	704	235	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	840	704	235	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	837	704	235	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=970;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	586	308	103	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	586	308	103	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=267;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=857;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	440	308	103	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	586	308	103	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	504	425	142	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	99	-	-	-	-	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=672;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=903;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	954	587	196	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	837	587	196	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	586	227	76	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	586	227	76	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	586	227	76	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	840	587	196	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	894	587	196	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	837	587	196	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127821	17:7674259-7674259	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	847	587	196	N/S	aAc/aGc	rs144340710,CM951230,COSV52700907,COSV52979785,COSV52987012	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,benign,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	714	572	191	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	572	572	191	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	572	572	191	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	705	572	191	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	708	572	191	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	705	572	191	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=270;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	454	176	59	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	454	176	59	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	828	-	-	-	-	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=157;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	308	176	59	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	454	176	59	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	372	293	98	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1372;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=203;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	822	455	152	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	705	455	152	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	454	95	32	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	454	95	32	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	454	95	32	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	708	455	152	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	762	455	152	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	705	455	152	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
127816	17:7674959-7674959	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	715	455	152	P/R	cCt/cGt	rs587778718,CD972478,COSV52729903,COSV52875587,COSV53423237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant,splice_region_variant	700	558	186	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant,splice_region_variant	558	558	186	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant,splice_region_variant	558	558	186	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant,splice_region_variant	691	558	186	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant,splice_region_variant	694	558	186	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant,splice_region_variant	691	558	186	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs375275361,COSV52677455,COSV53407442	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=175;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant,splice_region_variant	440	162	54	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant,splice_region_variant	440	162	54	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	814	-	-	-	-	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375275361,COSV52677455,COSV53407442	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=62;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant,splice_region_variant	294	162	54	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant,splice_region_variant	440	162	54	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant,splice_region_variant	358	279	93	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000574684.1	Transcript	splice_region_variant,non_coding_transcript_exon_variant	66	-	-	-	-	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs375275361,COSV52677455,COSV53407442	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1467;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375275361,COSV52677455,COSV53407442	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=108;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant,splice_region_variant	808	441	147	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant,splice_region_variant	691	441	147	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant,splice_region_variant	440	81	27	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant,splice_region_variant	440	81	27	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant,splice_region_variant	440	81	27	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant,splice_region_variant	694	441	147	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant,splice_region_variant	748	441	147	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant,splice_region_variant	691	441	147	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230006	17:7675054-7675054	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,splice_region_variant,NMD_transcript_variant	701	441	147	D/E	gaT/gaA	rs375275361,COSV52677455,COSV53407442	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	696	554	185	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	554	554	185	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	554	554	185	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	687	554	185	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	690	554	185	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	687	554	185	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=171;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	436	158	53	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	436	158	53	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	810	-	-	-	-	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=58;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	290	158	53	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	436	158	53	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	354	275	92	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	62	-	-	-	-	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1471;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=104;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	804	437	146	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	687	437	146	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	436	77	26	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	436	77	26	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	436	77	26	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	690	437	146	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	744	437	146	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	687	437	146	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
141359	17:7675058-7675058	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	697	437	146	S/N	aGc/aAc	rs150607408,COSV52891873,COSV53087101,COSV53685498	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	651	509	170	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	509	509	170	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	509	509	170	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	642	509	170	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	645	509	170	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	642	509	170	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=126;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	391	113	38	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	391	113	38	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	765	-	-	-	-	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=13;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	245	113	38	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	391	113	38	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	309	230	77	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	17	-	-	-	-	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1516;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=59;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	759	392	131	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	642	392	131	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	391	32	11	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	391	32	11	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	391	32	11	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	645	392	131	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	699	392	131	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	642	392	131	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
184014	17:7675103-7675103	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	652	392	131	T/M	aCg/aTg	rs779000871,CM125162,COSV52701457,COSV53143719,COSV99415505	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	622	480	160	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	480	480	160	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	480	480	160	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	613	480	160	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	616	480	160	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	613	480	160	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=97;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	362	84	28	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	362	84	28	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	736	-	-	-	-	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	618	480	160	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	216	84	28	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	362	84	28	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	280	201	67	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=13;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1545;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=30;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	730	363	121	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	613	363	121	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000610623.4	Transcript	start_lost	362	3	1	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000618944.4	Transcript	start_lost	362	3	1	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000619186.4	Transcript	start_lost	362	3	1	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	616	363	121	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	670	363	121	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	613	363	121	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
230758	17:7675132-7675132	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	623	363	121	M/I	atG/atA	rs772354334,COSV52849333,COSV53297171,COSV53424484,COSV53438638	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	611	469	157	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	469	469	157	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	469	469	157	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	602	469	157	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	605	469	157	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	602	469	157	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=86;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	351	73	25	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	351	73	25	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	725	-	-	-	-	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	607	469	157	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	205	73	25	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	351	73	25	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	269	190	64	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=24;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1556;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=19;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	719	352	118	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	602	352	118	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	351	-	-	-	-	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	351	-	-	-	-	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	351	-	-	-	-	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	605	352	118	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	659	352	118	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	602	352	118	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
185404	17:7675143-7675143	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	612	352	118	V/I	Gtc/Atc	rs121912654,CM137621,COSV52667015,COSV52676009,COSV52752314,COSV53205488	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	471	329	110	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	329	329	110	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	329	329	110	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	462	329	110	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	465	329	110	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	462	329	110	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	511	329	110	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	585	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	467	329	110	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=921;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2453;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	468	329	110	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	579	212	71	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	462	212	71	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	465	212	71	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	519	212	71	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	462	212	71	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
127808	17:7676040-7676040	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	472	212	71	R/H	cGt/cAt	rs11540654,CM115383,CM134053,CM984590,COSV52662399,COSV52668419,COSV52680444,COSV53132492	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,not_provided;SOMATIC=0,0,0,0,1,1,1,1;PHENO=1,1,1,1,1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	464	322	108	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	322	322	108	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	322	322	108	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	455	322	108	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	458	322	108	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	455	322	108	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	504	322	108	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=554;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=554;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	578	-	-	-	-	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	460	322	108	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=554;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=928;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2460;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	461	322	108	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	572	205	69	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	455	205	69	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=554;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=554;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=554;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	458	205	69	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	512	205	69	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	455	205	69	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
142431	17:7676047-7676047	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	465	205	69	G/S	Ggt/Agt	rs587782461,COSV104370760,COSV52862450,COSV52988774	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	461	319	107	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	319	319	107	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	319	319	107	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	452	319	107	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	455	319	107	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	452	319	107	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	501	319	107	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs368771578,COSV52679423,COSV53179040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=557;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs368771578,COSV52679423,COSV53179040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=557;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	575	-	-	-	-	rs368771578,COSV52679423,COSV53179040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	457	319	107	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs368771578,COSV52679423,COSV53179040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs368771578,COSV52679423,COSV53179040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=557;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs368771578,COSV52679423,COSV53179040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs368771578,COSV52679423,COSV53179040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=931;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs368771578,COSV52679423,COSV53179040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2463;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	458	319	107	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	569	202	68	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	452	202	68	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs368771578,COSV52679423,COSV53179040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=557;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs368771578,COSV52679423,COSV53179040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=557;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs368771578,COSV52679423,COSV53179040	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=557;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	455	202	68	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	509	202	68	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	452	202	68	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
140786	17:7676050-7676050	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	462	202	68	Y/H	Tac/Cac	rs368771578,COSV52679423,COSV53179040	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,uncertain_significance,benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	387	245	82	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	245	245	82	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	245	245	82	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	378	245	82	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	381	245	82	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	378	245	82	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	427	245	82	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs534447939,CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs534447939,CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	501	-	-	-	-	rs534447939,CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	383	245	82	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs534447939,CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs534447939,CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs534447939,CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs534447939,CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1005;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs534447939,CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2537;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	384	245	82	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	495	128	43	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	378	128	43	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs534447939,CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs534447939,CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs534447939,CM961375,COSV53209087	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	381	128	43	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	435	128	43	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	378	128	43	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
182946	17:7676124-7676124	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	388	128	43	P/L	cCg/cTg	rs534447939,CM961375,COSV53209087	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,uncertain_significance;SOMATIC=0,0,1;PHENO=1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	359	217	73	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	217	217	73	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	217	217	73	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	350	217	73	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	353	217	73	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	350	217	73	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	399	217	73	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	473	-	-	-	-	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	355	217	73	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1033;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2565;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	356	217	73	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	467	100	34	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	350	100	34	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	353	100	34	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	407	100	34	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	350	100	34	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
142386	17:7676152-7676152	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	360	100	34	V/M	Gtg/Atg	rs587782423,CD109812,COSV53023392,COSV53359933,COSV53361901,COSV53625318,COSV99409681	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,0,1,1,1,1,1;PHENO=1,1,1,1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	357	215	72	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	215	215	72	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	215	215	72	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	348	215	72	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	351	215	72	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	348	215	72	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	397	215	72	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	471	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	353	215	72	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1035;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2567;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	354	215	72	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	465	98	33	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	348	98	33	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	351	98	33	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	405	98	33	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	348	98	33	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
12351	17:7676154-7676154	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	358	98	33	P/R	cCc/cGc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,pathogenic;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	357	215	72	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	215	215	72	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	215	215	72	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	348	215	72	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	351	215	72	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	348	215	72	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	397	215	72	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	471	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	353	215	72	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1035;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2567;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	354	215	72	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	465	98	33	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	348	98	33	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	351	98	33	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	405	98	33	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	348	98	33	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
185120	17:7676154-7676154	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	358	98	33	P/H	cCc/cAc	rs1042522,CM961374,COSV52666208,COSV53098660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	330	188	63	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	188	188	63	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	188	188	63	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	321	188	63	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	324	188	63	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	321	188	63	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	370	188	63	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	444	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	326	188	63	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1062;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2594;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	327	188	63	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	438	71	24	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	321	71	24	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	324	71	24	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	378	71	24	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	321	71	24	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
182922	17:7676181-7676181	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	331	71	24	A/V	gCt/gTt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;PHENO=1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	329	187	63	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	187	187	63	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	187	187	63	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	320	187	63	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	323	187	63	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	320	187	63	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	369	187	63	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658902,COSV53504384,COSV53597306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=689;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658902,COSV53504384,COSV53597306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=689;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	443	-	-	-	-	rs876658902,COSV53504384,COSV53597306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	325	187	63	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876658902,COSV53504384,COSV53597306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658902,COSV53504384,COSV53597306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=689;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs876658902,COSV53504384,COSV53597306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658902,COSV53504384,COSV53597306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1063;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658902,COSV53504384,COSV53597306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2595;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	326	187	63	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	437	70	24	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	320	70	24	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658902,COSV53504384,COSV53597306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=689;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658902,COSV53504384,COSV53597306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=689;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658902,COSV53504384,COSV53597306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=689;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	323	70	24	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	377	70	24	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	320	70	24	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
231015	17:7676182-7676182	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	330	70	24	A/T	Gct/Act	rs876658902,COSV53504384,COSV53597306	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	287	145	49	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	145	145	49	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	145	145	49	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	278	145	49	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	281	145	49	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	278	145	49	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	327	145	49	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	401	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	283	145	49	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1105;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2637;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	284	145	49	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	395	28	10	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	278	28	10	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	281	28	10	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	335	28	10	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	278	28	10	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
135948	17:7676224-7676224	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	288	28	10	D/H	Gat/Cat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	287	145	49	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	145	145	49	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	145	145	49	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	278	145	49	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	281	145	49	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	278	145	49	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	327	145	49	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	401	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	283	145	49	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1105;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2637;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	284	145	49	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	395	28	10	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	278	28	10	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	281	28	10	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	335	28	10	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	278	28	10	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
186363	17:7676224-7676224	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	288	28	10	D/N	Gat/Aat	rs587780728,CM1610179,COSV52732514,COSV52864415,COSV52865140	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	281	139	47	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	139	139	47	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	139	139	47	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	272	139	47	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	275	139	47	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	272	139	47	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	321	139	47	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800371,CM052370,COSV53150763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=737;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800371,CM052370,COSV53150763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=737;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	395	-	-	-	-	rs1800371,CM052370,COSV53150763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	277	139	47	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1800371,CM052370,COSV53150763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800371,CM052370,COSV53150763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=737;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1800371,CM052370,COSV53150763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800371,CM052370,COSV53150763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1111;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800371,CM052370,COSV53150763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2643;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	278	139	47	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	389	22	8	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	272	22	8	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800371,CM052370,COSV53150763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=737;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800371,CM052370,COSV53150763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=737;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800371,CM052370,COSV53150763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=737;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	275	22	8	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	329	22	8	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	272	22	8	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
43588	17:7676230-7676230	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	282	22	8	P/S	Ccg/Tcg	rs1800371,CM052370,COSV53150763	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,0,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	247	105	35	L/F	ttG/ttC	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	105	105	35	L/F	ttG/ttC	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	105	105	35	L/F	ttG/ttC	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	238	105	35	L/F	ttG/ttC	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	241	105	35	L/F	ttG/ttC	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	238	105	35	L/F	ttG/ttC	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	287	105	35	L/F	ttG/ttC	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	361	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	243	105	35	L/F	ttG/ttC	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1145;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2677;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	244	105	35	L/F	ttG/ttC	rs121912661,COSV53067699,COSV53176324	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	355	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	238	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=771;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	241	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	295	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	238	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142562	17:7676264-7676264	G	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	248	-	-	-	-	rs121912661,COSV53067699,COSV53176324	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	170	28	10	V/I	Gtc/Atc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	28	28	10	V/I	Gtc/Atc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	28	28	10	V/I	Gtc/Atc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	161	28	10	V/I	Gtc/Atc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	164	28	10	V/I	Gtc/Atc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	161	28	10	V/I	Gtc/Atc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	210	28	10	V/I	Gtc/Atc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	167	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	166	28	10	V/I	Gtc/Atc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	107	28	10	V/I	Gtc/Atc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1448;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2980;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	167	28	10	V/I	Gtc/Atc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	161	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	161	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	164	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	218	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	161	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	171	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
127806	17:7676567-7676567	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000269305.9	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1189;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141499	ENST00000316024.9	Transcript	missense_variant	2379	31	11	P/S	Ccg/Tcg	rs17880282	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141499	ENST00000396463.7	Transcript	missense_variant	117	31	11	P/S	Ccg/Tcg	rs17880282	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000420246.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1198;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141499	ENST00000431639.6	Transcript	missense_variant	186	31	11	P/S	Ccg/Tcg	rs17880282	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000445888.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1192;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000455263.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1198;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141499	ENST00000457584.6	Transcript	missense_variant	196	31	11	P/S	Ccg/Tcg	rs17880282	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141499	ENST00000467699.5	Transcript	non_coding_transcript_exon_variant	117	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=retained_intron;EXON=2/9;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141499	ENST00000498311.5	Transcript	missense_variant,NMD_transcript_variant	994	31	11	P/S	Ccg/Tcg	rs17880282	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000503591.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1252;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000505014.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1192;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000509690.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1192;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000514944.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1252;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141499	ENST00000534050.5	Transcript	missense_variant	203	31	11	P/S	Ccg/Tcg	rs17880282	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000571370.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=2308;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000604348.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1192;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000610292.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1198;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000610538.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1198;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000619485.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1192;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000620739.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1141;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000622645.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1198;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141510	ENST00000635293.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=1188;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141499	ENST00000698742.1	Transcript	missense_variant	681	31	11	P/S	Ccg/Tcg	rs17880282	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141499	ENST00000698743.1	Transcript	missense_variant,NMD_transcript_variant	159	31	11	P/S	Ccg/Tcg	rs17880282	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141499	ENST00000698744.1	Transcript	missense_variant,NMD_transcript_variant	126	31	11	P/S	Ccg/Tcg	rs17880282	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141499	ENST00000698745.1	Transcript	missense_variant,NMD_transcript_variant	126	31	11	P/S	Ccg/Tcg	rs17880282	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141499	ENST00000698746.1	Transcript	missense_variant	116	31	11	P/S	Ccg/Tcg	rs17880282	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	ENSG00000141499	ENST00000698747.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=963;STRAND=1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
325650	17:7688679-7688679	T	-	ENSR00000090892	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs17880282	IMPACT=MODIFIER;BIOTYPE=promoter;CLIN_SIG=benign,likely_benign;PHENO=1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000269305.9	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1360;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141499	ENST00000316024.9	Transcript	missense_variant	2550	202	68	R/G	Cgg/Ggg	rs2287499,CM077855,COSV52834815	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141499	ENST00000396463.7	Transcript	missense_variant	288	202	68	R/G	Cgg/Ggg	rs2287499,CM077855,COSV52834815	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000420246.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1369;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141499	ENST00000431639.6	Transcript	missense_variant	357	202	68	R/G	Cgg/Ggg	rs2287499,CM077855,COSV52834815	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000445888.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1363;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000455263.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1369;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141499	ENST00000457584.6	Transcript	missense_variant	367	202	68	R/G	Cgg/Ggg	rs2287499,CM077855,COSV52834815	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141499	ENST00000467699.5	Transcript	non_coding_transcript_exon_variant	288	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=retained_intron;EXON=2/9;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141499	ENST00000498311.5	Transcript	missense_variant,NMD_transcript_variant	1165	202	68	R/G	Cgg/Ggg	rs2287499,CM077855,COSV52834815	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000503591.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1423;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000505014.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1363;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000509690.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1363;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000514944.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1423;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141499	ENST00000534050.5	Transcript	missense_variant	374	202	68	R/G	Cgg/Ggg	rs2287499,CM077855,COSV52834815	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000571370.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=2479;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000604348.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1363;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000610292.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1369;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000610538.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1369;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000619485.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1363;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000620739.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1312;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000622645.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1369;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141510	ENST00000635293.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=1359;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141499	ENST00000698742.1	Transcript	missense_variant	852	202	68	R/G	Cgg/Ggg	rs2287499,CM077855,COSV52834815	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141499	ENST00000698743.1	Transcript	missense_variant,NMD_transcript_variant	330	202	68	R/G	Cgg/Ggg	rs2287499,CM077855,COSV52834815	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141499	ENST00000698744.1	Transcript	missense_variant,NMD_transcript_variant	297	202	68	R/G	Cgg/Ggg	rs2287499,CM077855,COSV52834815	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141499	ENST00000698745.1	Transcript	missense_variant,NMD_transcript_variant	297	202	68	R/G	Cgg/Ggg	rs2287499,CM077855,COSV52834815	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141499	ENST00000698746.1	Transcript	missense_variant	287	202	68	R/G	Cgg/Ggg	rs2287499,CM077855,COSV52834815	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	ENSG00000141499	ENST00000698747.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=792;STRAND=1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261001	17:7688850-7688850	G	-	ENSR00000090892	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2287499,CM077855,COSV52834815	IMPACT=MODIFIER;BIOTYPE=promoter;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000269305.9	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1565;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141499	ENST00000316024.9	Transcript	missense_variant	2755	407	136	P/R	cCc/cGc	rs34067256	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141499	ENST00000396463.7	Transcript	missense_variant	493	407	136	P/R	cCc/cGc	rs34067256	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000420246.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1574;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141499	ENST00000431639.6	Transcript	missense_variant	562	407	136	P/R	cCc/cGc	rs34067256	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000445888.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1568;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000455263.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1574;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141499	ENST00000457584.6	Transcript	missense_variant	572	407	136	P/R	cCc/cGc	rs34067256	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141499	ENST00000467699.5	Transcript	non_coding_transcript_exon_variant	493	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=retained_intron;EXON=2/9;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141499	ENST00000498311.5	Transcript	missense_variant,NMD_transcript_variant	1370	407	136	P/R	cCc/cGc	rs34067256	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000503591.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1628;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000505014.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1568;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000509690.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1568;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000514944.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1628;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141499	ENST00000534050.5	Transcript	missense_variant	579	407	136	P/R	cCc/cGc	rs34067256	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000571370.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=2684;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000604348.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1568;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000610292.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1574;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000610538.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1574;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000619485.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1568;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000620739.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1517;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000622645.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1574;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141510	ENST00000635293.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=1564;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141499	ENST00000698742.1	Transcript	missense_variant	1057	407	136	P/R	cCc/cGc	rs34067256	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141499	ENST00000698743.1	Transcript	missense_variant,NMD_transcript_variant	535	407	136	P/R	cCc/cGc	rs34067256	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141499	ENST00000698744.1	Transcript	missense_variant,NMD_transcript_variant	502	407	136	P/R	cCc/cGc	rs34067256	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141499	ENST00000698745.1	Transcript	missense_variant,NMD_transcript_variant	502	407	136	P/R	cCc/cGc	rs34067256	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=2/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141499	ENST00000698746.1	Transcript	missense_variant	492	407	136	P/R	cCc/cGc	rs34067256	IMPACT=MODERATE;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	ENSG00000141499	ENST00000698747.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=587;STRAND=1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
261002	17:7689055-7689055	G	-	ENSR00000090892	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs34067256	IMPACT=MODIFIER;BIOTYPE=promoter;CLIN_SIG=benign,likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=530;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=530;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1695;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=530;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=530;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925574	17:7667874-7667874	C	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1049800949	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=541;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=524;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=541;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=524;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1689;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=524;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=541;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=524;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926695	17:7667880-7667880	A	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2072740569	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=516;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=516;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=514;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=514;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=514;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1681;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=514;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=516;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=514;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=514;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=514;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=514;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=516;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925707	17:7667888-7667888	A	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2072740671	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=505;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=505;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=503;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=503;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=503;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1670;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=503;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=505;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=503;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=503;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=503;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=503;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=505;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920680	17:7667899-7667899	C	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs886596112	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=520;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=503;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=520;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=503;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1668;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=503;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=520;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=503;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927570	17:7667901-7667901	T	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2072740794	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=517;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=517;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1665;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=517;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921740	17:7667904-7667904	T	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1460750940	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=515;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=515;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1663;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=515;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919907	17:7667906-7667906	A	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=515;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=515;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1663;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=515;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=498;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925434	17:7667906-7667906	T	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs34785536	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=513;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=513;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1661;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=513;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
490169	17:7667908-7667908	A	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs183153328	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=512;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=495;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=512;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=495;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1660;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=495;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=512;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=495;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
925896	17:7667909-7667909	T	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2072741412	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=511;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=511;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=492;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=492;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=492;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1659;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=492;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=492;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=492;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=492;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=511;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=492;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919110	17:7667910-7667910	A	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2072741476	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=495;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=478;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=495;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=478;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=476;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=476;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=476;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1643;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=476;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=478;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=476;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=476;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=476;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=495;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=476;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=478;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927304	17:7667926-7667926	T	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2072741801	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=492;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=475;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=492;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=475;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=473;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=473;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=473;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1640;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=473;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=475;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=473;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=473;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=473;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=492;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=473;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=475;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920533	17:7667929-7667929	T	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs895577952	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=488;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=471;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=488;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=471;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=469;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=469;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=469;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1636;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=469;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=471;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=469;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=469;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=469;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=488;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=469;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=471;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927401	17:7667933-7667933	T	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs957784209,COSV53152118	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=287;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=270;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=287;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=270;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=268;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=268;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=268;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1435;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=268;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=270;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=268;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=268;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=268;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=287;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=268;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=270;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1294447	17:7668134-7668134	A	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1614984	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=251;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=234;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=251;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=234;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=232;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=232;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=232;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1399;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=232;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=234;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=232;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=232;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=232;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=251;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=232;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=234;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1170064	17:7668169-7668169	GCCGTG	-	ENSR00001006477	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs17880560	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000269305.9	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=33;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000420246.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=16;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000445888.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=33;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000455263.6	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=16;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000504290.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000504937.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000510385.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1181;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000610292.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000610538.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=16;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000610623.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000618944.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000619186.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000619485.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=33;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000620739.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000622645.4	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=16;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
369233	17:7668388-7668388	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs17883782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000269305.9	Transcript	3_prime_UTR_variant	2394	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	2518	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000445888.6	Transcript	3_prime_UTR_variant	2388	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	2445	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	2194	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000504937.5	Transcript	3_prime_UTR_variant	2134	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4996;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	2267	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000610292.4	Transcript	3_prime_UTR_variant	2502	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	2445	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	2194	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	2267	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000619186.4	Transcript	3_prime_UTR_variant	2134	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000619485.4	Transcript	3_prime_UTR_variant	2388	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000620739.4	Transcript	3_prime_UTR_variant	2442	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	2518	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325620	17:7668539-7668539	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs114831472	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000269305.9	Transcript	3_prime_UTR_variant	2260	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	2384	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000445888.6	Transcript	3_prime_UTR_variant	2254	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	2311	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	2060	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000504937.5	Transcript	3_prime_UTR_variant	2000	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4862;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	2133	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=896;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000610292.4	Transcript	3_prime_UTR_variant	2368	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	2311	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	2060	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	2133	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000619186.4	Transcript	3_prime_UTR_variant	2000	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000619485.4	Transcript	3_prime_UTR_variant	2254	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000620739.4	Transcript	3_prime_UTR_variant	2308	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	2384	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325622	17:7668673-7668673	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs55817367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000269305.9	Transcript	3_prime_UTR_variant	2150	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	2274	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000445888.6	Transcript	3_prime_UTR_variant	2144	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	2201	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1950	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000504937.5	Transcript	3_prime_UTR_variant	1890	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4752;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	2023	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=786;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000610292.4	Transcript	3_prime_UTR_variant	2258	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	2201	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1950	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	2023	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000619186.4	Transcript	3_prime_UTR_variant	1890	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000619485.4	Transcript	3_prime_UTR_variant	2144	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000620739.4	Transcript	3_prime_UTR_variant	2198	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	2274	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325623	17:7668783-7668783	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs17884306	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000269305.9	Transcript	3_prime_UTR_variant	2097	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	2221	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000445888.6	Transcript	3_prime_UTR_variant	2091	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	2148	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1897	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000504937.5	Transcript	3_prime_UTR_variant	1837	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4699;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1970	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=733;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000610292.4	Transcript	3_prime_UTR_variant	2205	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	2148	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1897	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1970	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000619186.4	Transcript	3_prime_UTR_variant	1837	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000619485.4	Transcript	3_prime_UTR_variant	2091	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000620739.4	Transcript	3_prime_UTR_variant	2145	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	2221	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325627	17:7668836-7668836	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs200378797	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000269305.9	Transcript	3_prime_UTR_variant	1937	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	2061	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000445888.6	Transcript	3_prime_UTR_variant	1931	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1988	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1737	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000504937.5	Transcript	3_prime_UTR_variant	1677	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4539;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1810	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=573;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000610292.4	Transcript	3_prime_UTR_variant	2045	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1988	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1737	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1810	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000619186.4	Transcript	3_prime_UTR_variant	1677	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000619485.4	Transcript	3_prime_UTR_variant	1931	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000620739.4	Transcript	3_prime_UTR_variant	1985	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	2061	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325633	17:7668996-7668996	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs17879353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000269305.9	Transcript	3_prime_UTR_variant	1893-1894	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	2017-2018	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000445888.6	Transcript	3_prime_UTR_variant	1887-1888	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1944-1945	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1693-1694	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000504937.5	Transcript	3_prime_UTR_variant	1633-1634	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4495;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1766-1767	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=529;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000610292.4	Transcript	3_prime_UTR_variant	2001-2002	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1944-1945	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1693-1694	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1766-1767	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000619186.4	Transcript	3_prime_UTR_variant	1633-1634	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000619485.4	Transcript	3_prime_UTR_variant	1887-1888	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000620739.4	Transcript	3_prime_UTR_variant	1941-1942	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	2017-2018	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325634	17:7669038-7669040	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555523911	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000269305.9	Transcript	3_prime_UTR_variant	1809	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1933	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000445888.6	Transcript	3_prime_UTR_variant	1803	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1860	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1609	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000504937.5	Transcript	3_prime_UTR_variant	1549	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4411;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1682	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=445;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000610292.4	Transcript	3_prime_UTR_variant	1917	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1860	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1609	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1682	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000619186.4	Transcript	3_prime_UTR_variant	1549	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000619485.4	Transcript	3_prime_UTR_variant	1803	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000620739.4	Transcript	3_prime_UTR_variant	1857	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1933	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325637	17:7669124-7669124	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs4968187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000269305.9	Transcript	3_prime_UTR_variant	1733	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1857	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000445888.6	Transcript	3_prime_UTR_variant	1727	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1784	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1533	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000504937.5	Transcript	3_prime_UTR_variant	1473	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4335;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1606	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=369;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000610292.4	Transcript	3_prime_UTR_variant	1841	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1784	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1533	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1606	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000619186.4	Transcript	3_prime_UTR_variant	1473	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000619485.4	Transcript	3_prime_UTR_variant	1727	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000620739.4	Transcript	3_prime_UTR_variant	1781	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1857	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891532	17:7669200-7669200	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs191918079,COSV53538698	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000269305.9	Transcript	3_prime_UTR_variant	1681	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1805	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000445888.6	Transcript	3_prime_UTR_variant	1675	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1732	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1481	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000504937.5	Transcript	3_prime_UTR_variant	1421	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4283;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1554	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4965;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=317;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000610292.4	Transcript	3_prime_UTR_variant	1789	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1732	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1481	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1554	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000619186.4	Transcript	3_prime_UTR_variant	1421	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000619485.4	Transcript	3_prime_UTR_variant	1675	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000620739.4	Transcript	3_prime_UTR_variant	1729	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1805	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891533	17:7669252-7669252	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs534624315	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000269305.9	Transcript	3_prime_UTR_variant	1652	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1776	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000445888.6	Transcript	3_prime_UTR_variant	1646	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1703	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1452	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000504937.5	Transcript	3_prime_UTR_variant	1392	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4254;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1525	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4936;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4973;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=288;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000610292.4	Transcript	3_prime_UTR_variant	1760	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1703	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1452	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1525	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000619186.4	Transcript	3_prime_UTR_variant	1392	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000619485.4	Transcript	3_prime_UTR_variant	1646	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000620739.4	Transcript	3_prime_UTR_variant	1700	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1776	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
891534	17:7669281-7669281	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs17881366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000269305.9	Transcript	3_prime_UTR_variant	1529	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1653	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000445888.6	Transcript	3_prime_UTR_variant	1523	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1580	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1329	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000504937.5	Transcript	3_prime_UTR_variant	1269	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4131;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1402	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4813;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4850;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000576024.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=165;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000610292.4	Transcript	3_prime_UTR_variant	1637	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1580	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1329	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1402	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000619186.4	Transcript	3_prime_UTR_variant	1269	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000619485.4	Transcript	3_prime_UTR_variant	1523	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000620739.4	Transcript	3_prime_UTR_variant	1577	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1653	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
325642	17:7669404-7669404	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs16956880	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000269305.9	Transcript	3_prime_UTR_variant	1339	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1463	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000445888.6	Transcript	3_prime_UTR_variant	1333	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1390	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1139	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000504937.5	Transcript	3_prime_UTR_variant	1079	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4932;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3941;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1212	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4623;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	150	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000610292.4	Transcript	3_prime_UTR_variant	1447	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1390	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1139	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1212	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000619186.4	Transcript	3_prime_UTR_variant	1079	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000619485.4	Transcript	3_prime_UTR_variant	1333	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000620739.4	Transcript	3_prime_UTR_variant	1387	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1463	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384516	17:7669594-7669594	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs374294340	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000269305.9	Transcript	3_prime_UTR_variant	1337	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1461	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000445888.6	Transcript	3_prime_UTR_variant	1331	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1388	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1137	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000504937.5	Transcript	3_prime_UTR_variant	1077	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4930;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3939;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1210	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4621;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4658;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	148	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000610292.4	Transcript	3_prime_UTR_variant	1445	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1388	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1137	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1210	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000619186.4	Transcript	3_prime_UTR_variant	1077	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000619485.4	Transcript	3_prime_UTR_variant	1331	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000620739.4	Transcript	3_prime_UTR_variant	1385	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1461	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380960	17:7669596-7669596	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1057520915	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1321	1179	393	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1445	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1315	1179	393	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1372	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1121	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	1061	783	261	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4914;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3923;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1194	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4605;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4642;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	132	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1429	1062	354	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1372	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1121	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1194	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	1061	702	234	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1315	1062	354	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1369	1062	354	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1445	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1559869	17:7669612-7669612	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1319	1177	393	D/Y	Gac/Tac	rs1192921623,COSV105024787	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1443	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1313	1177	393	D/Y	Gac/Tac	rs1192921623,COSV105024787	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1370	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1119	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1059	781	261	D/Y	Gac/Tac	rs1192921623,COSV105024787	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4912;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3921;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1192	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4603;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4640;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	130	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1427	1060	354	D/Y	Gac/Tac	rs1192921623,COSV105024787	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1370	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1119	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1192	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1059	700	234	D/Y	Gac/Tac	rs1192921623,COSV105024787	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1313	1060	354	D/Y	Gac/Tac	rs1192921623,COSV105024787	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1367	1060	354	D/Y	Gac/Tac	rs1192921623,COSV105024787	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1443	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1741120	17:7669614-7669614	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1192921623,COSV105024787	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1315	1173	391	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1439	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1309	1173	391	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1366	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1115	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	1055	777	259	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4908;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3917;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1188	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4599;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4636;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	126	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1423	1056	352	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1366	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1115	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1188	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	1055	696	232	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1309	1056	352	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1363	1056	352	D	gaC/gaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1439	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1547237	17:7669618-7669618	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1309	1167	389	G	ggG/ggT	rs1597345246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1433	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1303	1167	389	G	ggG/ggT	rs1597345246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1360	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1109	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	1049	771	257	G	ggG/ggT	rs1597345246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4902;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3911;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1182	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4593;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	120	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1417	1050	350	G	ggG/ggT	rs1597345246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1360	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1109	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1182	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	1049	690	230	G	ggG/ggT	rs1597345246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1303	1050	350	G	ggG/ggT	rs1597345246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1357	1050	350	G	ggG/ggT	rs1597345246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1433	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762432	17:7669624-7669624	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1597345246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1306	1164	388	E/D	gaA/gaT	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1430	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1300	1164	388	E/D	gaA/gaT	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1357	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1106	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1046	768	256	E/D	gaA/gaT	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4899;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3908;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1179	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4590;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	117	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1414	1047	349	E/D	gaA/gaT	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1357	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1106	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1179	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1046	687	229	E/D	gaA/gaT	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1300	1047	349	E/D	gaA/gaT	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1354	1047	349	E/D	gaA/gaT	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1430	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737684	17:7669627-7669627	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1305	1163	388	E/A	gAa/gCa	rs587781736,CM160112,COSV99037201	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1429	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1299	1163	388	E/A	gAa/gCa	rs587781736,CM160112,COSV99037201	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1356	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1105	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1045	767	256	E/A	gAa/gCa	rs587781736,CM160112,COSV99037201	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4898;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3907;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1178	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4589;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4626;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	116	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1413	1046	349	E/A	gAa/gCa	rs587781736,CM160112,COSV99037201	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1356	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1105	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1178	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1045	686	229	E/A	gAa/gCa	rs587781736,CM160112,COSV99037201	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1299	1046	349	E/A	gAa/gCa	rs587781736,CM160112,COSV99037201	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1353	1046	349	E/A	gAa/gCa	rs587781736,CM160112,COSV99037201	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1429	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
141425	17:7669628-7669628	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs587781736,CM160112,COSV99037201	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1304	1162	388	E/Q	Gaa/Caa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1428	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1298	1162	388	E/Q	Gaa/Caa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1355	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1104	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1044	766	256	E/Q	Gaa/Caa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4897;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3906;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1177	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4588;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4625;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	115	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1412	1045	349	E/Q	Gaa/Caa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1355	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1104	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1177	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1044	685	229	E/Q	Gaa/Caa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1298	1045	349	E/Q	Gaa/Caa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1352	1045	349	E/Q	Gaa/Caa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1428	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1737291	17:7669629-7669629	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1303	1161	387	T	acA/acG	rs1131691017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1427	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1297	1161	387	T	acA/acG	rs1131691017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1354	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1103	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	1043	765	255	T	acA/acG	rs1131691017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4896;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3905;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1176	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4587;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4624;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	114	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1411	1044	348	T	acA/acG	rs1131691017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1354	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1103	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1176	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	1043	684	228	T	acA/acG	rs1131691017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1297	1044	348	T	acA/acG	rs1131691017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1351	1044	348	T	acA/acG	rs1131691017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1427	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
428878	17:7669630-7669630	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1131691017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1299	1157	386	K/R	aAg/aGg	rs1597345314	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1423	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1293	1157	386	K/R	aAg/aGg	rs1597345314	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1350	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1099	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1039	761	254	K/R	aAg/aGg	rs1597345314	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3901;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1172	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4583;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4620;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	110	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1407	1040	347	K/R	aAg/aGg	rs1597345314	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1350	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1099	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1172	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1039	680	227	K/R	aAg/aGg	rs1597345314	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1293	1040	347	K/R	aAg/aGg	rs1597345314	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1347	1040	347	K/R	aAg/aGg	rs1597345314	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1423	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
818446	17:7669634-7669634	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1597345314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1297	1155	385	F/L	ttC/ttA	COSV99378860	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1421	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1291	1155	385	F/L	ttC/ttA	COSV99378860	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1348	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1097	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1037	759	253	F/L	ttC/ttA	COSV99378860	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4890;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3899;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1170	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4581;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4618;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	108	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1405	1038	346	F/L	ttC/ttA	COSV99378860	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1348	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1097	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1170	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1037	678	226	F/L	ttC/ttA	COSV99378860	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1291	1038	346	F/L	ttC/ttA	COSV99378860	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1345	1038	346	F/L	ttC/ttA	COSV99378860	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1421	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735082	17:7669636-7669636	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1297	1155	385	F	ttC/ttT	COSV99378860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1421	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1291	1155	385	F	ttC/ttT	COSV99378860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1348	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1097	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	1037	759	253	F	ttC/ttT	COSV99378860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4890;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3899;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1170	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4581;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4618;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	108	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1405	1038	346	F	ttC/ttT	COSV99378860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1348	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1097	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1170	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	1037	678	226	F	ttC/ttT	COSV99378860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1291	1038	346	F	ttC/ttT	COSV99378860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1345	1038	346	F	ttC/ttT	COSV99378860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1421	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735146	17:7669636-7669636	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	COSV99378860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1295	1153	385	F/L	Ttc/Ctc	rs1555524094,COSV53389349	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1419	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1289	1153	385	F/L	Ttc/Ctc	rs1555524094,COSV53389349	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1346	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1095	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1035	757	253	F/L	Ttc/Ctc	rs1555524094,COSV53389349	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4888;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3897;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1168	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4579;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4616;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	106	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1403	1036	346	F/L	Ttc/Ctc	rs1555524094,COSV53389349	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1346	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1095	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1168	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1035	676	226	F/L	Ttc/Ctc	rs1555524094,COSV53389349	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1289	1036	346	F/L	Ttc/Ctc	rs1555524094,COSV53389349	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1343	1036	346	F/L	Ttc/Ctc	rs1555524094,COSV53389349	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1419	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
485029	17:7669638-7669638	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555524094,COSV53389349	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1293	1151	384	M/T	aTg/aCg	rs1060501196	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1417	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1287	1151	384	M/T	aTg/aCg	rs1060501196	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1344	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1093	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1033	755	252	M/T	aTg/aCg	rs1060501196	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4886;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3895;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1166	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4577;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4614;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	104	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1401	1034	345	M/T	aTg/aCg	rs1060501196	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1344	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1093	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1166	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1033	674	225	M/T	aTg/aCg	rs1060501196	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1287	1034	345	M/T	aTg/aCg	rs1060501196	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1341	1034	345	M/T	aTg/aCg	rs1060501196	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1417	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406575	17:7669640-7669640	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1060501196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1292	1150	384	M/V	Atg/Gtg	rs730882009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1416	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1286	1150	384	M/V	Atg/Gtg	rs730882009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1343	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1092	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1032	754	252	M/V	Atg/Gtg	rs730882009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4885;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3894;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1165	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4576;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4613;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	103	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1400	1033	345	M/V	Atg/Gtg	rs730882009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1343	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1092	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1165	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1032	673	225	M/V	Atg/Gtg	rs730882009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1286	1033	345	M/V	Atg/Gtg	rs730882009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1340	1033	345	M/V	Atg/Gtg	rs730882009	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1416	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
182939	17:7669641-7669641	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs730882009	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1291	1149	383	L	ctC/ctT	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1415	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1285	1149	383	L	ctC/ctT	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1342	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1091	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	1031	753	251	L	ctC/ctT	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4884;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3893;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1164	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4575;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4612;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	102	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1399	1032	344	L	ctC/ctT	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1342	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1091	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1164	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	1031	672	224	L	ctC/ctT	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1285	1032	344	L	ctC/ctT	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1339	1032	344	L	ctC/ctT	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1415	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
183740	17:7669642-7669642	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,benign/likely_benign,likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1291	1149	383	L	ctC/ctA	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1415	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1285	1149	383	L	ctC/ctA	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1342	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1091	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	1031	753	251	L	ctC/ctA	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4884;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3893;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1164	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4575;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4612;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000576024.1	Transcript	3_prime_UTR_variant	102	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1399	1032	344	L	ctC/ctA	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1342	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1091	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1164	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	1031	672	224	L	ctC/ctA	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1285	1032	344	L	ctC/ctA	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1339	1032	344	L	ctC/ctA	rs373710656	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1415	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482224	17:7669642-7669642	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs373710656	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1279	1137	379	R	cgC/cgT	rs786202368,COSV53292005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1403	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1273	1137	379	R	cgC/cgT	rs786202368,COSV53292005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1330	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1079	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	1019	741	247	R	cgC/cgT	rs786202368,COSV53292005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4872;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3881;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1152	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4563;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4600;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant	90	91	31	P/S	Cca/Tca	rs786202368,COSV53292005	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1387	1020	340	R	cgC/cgT	rs786202368,COSV53292005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1330	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1079	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1152	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	1019	660	220	R	cgC/cgT	rs786202368,COSV53292005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1273	1020	340	R	cgC/cgT	rs786202368,COSV53292005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1327	1020	340	R	cgC/cgT	rs786202368,COSV53292005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1403	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185679	17:7669654-7669654	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs786202368,COSV53292005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1278	1136	379	R/L	cGc/cTc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1402	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1272	1136	379	R/L	cGc/cTc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1329	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1078	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1018	740	247	R/L	cGc/cTc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4871;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3880;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1151	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4562;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000576024.1	Transcript	synonymous_variant	89	90	30	P	ccG/ccT	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1386	1019	340	R/L	cGc/cTc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1329	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1078	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1151	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1018	659	220	R/L	cGc/cTc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1272	1019	340	R/L	cGc/cTc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1326	1019	340	R/L	cGc/cTc	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1402	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
216463	17:7669655-7669655	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs863224682,CM156902,COSV52708084,COSV52708100	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1277	1135	379	R/S	Cgc/Agc	rs749061599,CM1612945,COSV53033101	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1401	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1271	1135	379	R/S	Cgc/Agc	rs749061599,CM1612945,COSV53033101	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1328	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1077	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1017	739	247	R/S	Cgc/Agc	rs749061599,CM1612945,COSV53033101	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4870;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3879;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1150	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4561;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4598;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant	88	89	30	P/Q	cCg/cAg	rs749061599,CM1612945,COSV53033101	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1385	1018	340	R/S	Cgc/Agc	rs749061599,CM1612945,COSV53033101	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1328	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1077	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1150	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1017	658	220	R/S	Cgc/Agc	rs749061599,CM1612945,COSV53033101	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1271	1018	340	R/S	Cgc/Agc	rs749061599,CM1612945,COSV53033101	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1325	1018	340	R/S	Cgc/Agc	rs749061599,CM1612945,COSV53033101	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1401	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
186762	17:7669656-7669656	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs749061599,CM1612945,COSV53033101	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1276	1134	378	S	tcC/tcT	rs1060504165	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1400	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1270	1134	378	S	tcC/tcT	rs1060504165	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1327	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1076	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	1016	738	246	S	tcC/tcT	rs1060504165	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4869;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3878;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1149	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4560;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant	87	88	30	P/S	Ccg/Tcg	rs1060504165	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1384	1017	339	S	tcC/tcT	rs1060504165	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1327	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1076	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1149	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	1016	657	219	S	tcC/tcT	rs1060504165	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1270	1017	339	S	tcC/tcT	rs1060504165	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1324	1017	339	S	tcC/tcT	rs1060504165	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1400	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414033	17:7669657-7669657	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1060504165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1273	1131	377	T	acC/acA	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1397	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1267	1131	377	T	acC/acA	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1324	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1073	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	1013	735	245	T	acC/acA	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4866;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3875;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1146	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4557;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant	84	85	29	L/I	Ctc/Atc	rs1456836660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1381	1014	338	T	acC/acA	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1324	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1073	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1146	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	1013	654	218	T	acC/acA	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1267	1014	338	T	acC/acA	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1321	1014	338	T	acC/acA	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1397	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511854	17:7669660-7669660	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1273	1131	377	T	acC/acT	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1397	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1267	1131	377	T	acC/acT	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1324	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1073	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	1013	735	245	T	acC/acT	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4866;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3875;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1146	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4557;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant	84	85	29	L/F	Ctc/Ttc	rs1456836660	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1381	1014	338	T	acC/acT	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1324	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1073	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1146	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	1013	654	218	T	acC/acT	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1267	1014	338	T	acC/acT	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1321	1014	338	T	acC/acT	rs1456836660	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1397	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
745265	17:7669660-7669660	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1456836660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1267	1125	375	Q	caG/caA	rs764011631,CD1617857,COSV105874506	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1391	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1261	1125	375	Q	caG/caA	rs764011631,CD1617857,COSV105874506	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1318	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1067	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	1007	729	243	Q	caG/caA	rs764011631,CD1617857,COSV105874506	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4860;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3869;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1140	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4551;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant	78	79	27	V/I	Gtc/Atc	rs764011631,CD1617857,COSV105874506	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1375	1008	336	Q	caG/caA	rs764011631,CD1617857,COSV105874506	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1318	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1067	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1140	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	1007	648	216	Q	caG/caA	rs764011631,CD1617857,COSV105874506	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1261	1008	336	Q	caG/caA	rs764011631,CD1617857,COSV105874506	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1315	1008	336	Q	caG/caA	rs764011631,CD1617857,COSV105874506	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1391	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
629927	17:7669666-7669666	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs764011631,CD1617857,COSV105874506	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1265	1123	375	Q/K	Cag/Aag	COSV52716070,COSV52776099	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1389	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1259	1123	375	Q/K	Cag/Aag	COSV52716070,COSV52776099	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1316	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1065	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1005	727	243	Q/K	Cag/Aag	COSV52716070,COSV52776099	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3867;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1138	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4549;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4586;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000576024.1	Transcript	stop_gained	76	77	26	S/*	tCa/tAa	COSV52716070,COSV52776099	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1373	1006	336	Q/K	Cag/Aag	COSV52716070,COSV52776099	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1316	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1065	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1138	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1005	646	216	Q/K	Cag/Aag	COSV52716070,COSV52776099	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1259	1006	336	Q/K	Cag/Aag	COSV52716070,COSV52776099	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1313	1006	336	Q/K	Cag/Aag	COSV52716070,COSV52776099	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1389	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1798385	17:7669668-7669668	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	COSV52716070,COSV52776099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1263	1121	374	G/V	gGt/gTt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1387	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1257	1121	374	G/V	gGt/gTt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1314	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1063	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1003	725	242	G/V	gGt/gTt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4856;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3865;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1136	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4547;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4584;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000576024.1	Transcript	synonymous_variant	74	75	25	G	ggG/ggT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1371	1004	335	G/V	gGt/gTt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1314	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1063	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1136	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1003	644	215	G/V	gGt/gTt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1257	1004	335	G/V	gGt/gTt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1311	1004	335	G/V	gGt/gTt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1387	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1797938	17:7669670-7669670	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1262	1120	374	G/R	Ggt/Cgt	rs587781858,COSV53311139	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1386	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1256	1120	374	G/R	Ggt/Cgt	rs587781858,COSV53311139	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1313	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1062	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	1002	724	242	G/R	Ggt/Cgt	rs587781858,COSV53311139	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4855;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3864;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1135	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4546;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4583;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant	73	74	25	G/A	gGg/gCg	rs587781858,COSV53311139	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1370	1003	335	G/R	Ggt/Cgt	rs587781858,COSV53311139	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1313	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1062	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1135	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	1002	643	215	G/R	Ggt/Cgt	rs587781858,COSV53311139	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1256	1003	335	G/R	Ggt/Cgt	rs587781858,COSV53311139	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1310	1003	335	G/R	Ggt/Cgt	rs587781858,COSV53311139	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1386	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
230269	17:7669671-7669671	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs587781858,COSV53311139	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1261	1119	373	K	aaG/aaA	rs1342613419,COSV105878345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1385	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1255	1119	373	K	aaG/aaA	rs1342613419,COSV105878345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1312	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1061	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	1001	723	241	K	aaG/aaA	rs1342613419,COSV105878345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4854;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3863;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1134	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4545;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4582;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant	72	73	25	G/R	Ggg/Agg	rs1342613419,COSV105878345	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1369	1002	334	K	aaG/aaA	rs1342613419,COSV105878345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1312	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1061	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1134	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	1001	642	214	K	aaG/aaA	rs1342613419,COSV105878345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1255	1002	334	K	aaG/aaA	rs1342613419,COSV105878345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1309	1002	334	K	aaG/aaA	rs1342613419,COSV105878345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1385	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628429	17:7669672-7669672	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1342613419,COSV105878345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1255	1113	371	S	tcC/tcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1379	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1249	1113	371	S	tcC/tcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1306	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1055	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	995	717	239	S	tcC/tcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4848;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3857;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1128	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4539;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4576;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000576024.1	Transcript	stop_gained	66	67	23	Q/*	Caa/Taa	-	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1363	996	332	S	tcC/tcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1306	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1055	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1128	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	995	636	212	S	tcC/tcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1249	996	332	S	tcC/tcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1303	996	332	S	tcC/tcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1379	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919471	17:7669678-7669678	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1252	1110	370	K	aaG/aaA	rs1567540533	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1376	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1246	1110	370	K	aaG/aaA	rs1567540533	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1303	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1052	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	992	714	238	K	aaG/aaA	rs1567540533	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4845;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3854;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1125	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4536;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4573;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant	63	64	22	V/I	Gtc/Atc	rs1567540533	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1360	993	331	K	aaG/aaA	rs1567540533	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1303	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1052	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1125	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	992	633	211	K	aaG/aaA	rs1567540533	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1246	993	331	K	aaG/aaA	rs1567540533	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1300	993	331	K	aaG/aaA	rs1567540533	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1376	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628982	17:7669681-7669681	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567540533	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1249	1107	369	L	ctG/ctA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1373	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1243	1107	369	L	ctG/ctA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1300	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1049	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	989	711	237	L	ctG/ctA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4842;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3851;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1122	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4533;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4570;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant	60	61	21	E/K	Gaa/Aaa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1357	990	330	L	ctG/ctA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1300	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1049	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1122	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	989	630	210	L	ctG/ctA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1243	990	330	L	ctG/ctA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1297	990	330	L	ctG/ctA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1373	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1138543	17:7669684-7669684	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1246	1104	368	H	caC/caT	rs1289241865	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1370	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1240	1104	368	H	caC/caT	rs1289241865	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1297	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1046	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	986	708	236	H	caC/caT	rs1289241865	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4839;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3848;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1119	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4530;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4567;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant	57	58	20	P/S	Cct/Tct	rs1289241865	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1354	987	329	H	caC/caT	rs1289241865	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1297	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1046	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1119	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	986	627	209	H	caC/caT	rs1289241865	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1240	987	329	H	caC/caT	rs1289241865	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1294	987	329	H	caC/caT	rs1289241865	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1370	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485042	17:7669687-7669687	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1289241865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant,splice_region_variant	1244	1102	368	H/Y	Cac/Tac	rs786204227	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs786204227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs786204227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,3_prime_UTR_variant	1368	-	-	-	-	rs786204227	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant,splice_region_variant	1238	1102	368	H/Y	Cac/Tac	rs786204227	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,3_prime_UTR_variant	1295	-	-	-	-	rs786204227	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,3_prime_UTR_variant	1044	-	-	-	-	rs786204227	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant,splice_region_variant	984	706	236	H/Y	Cac/Tac	rs786204227	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786204227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4837;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786204227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3846;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,3_prime_UTR_variant	1117	-	-	-	-	rs786204227	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786204227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4528;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786204227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4565;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant,splice_region_variant	55	56	19	P/L	cCa/cTa	rs786204227	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant,splice_region_variant	1352	985	329	H/Y	Cac/Tac	rs786204227	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,3_prime_UTR_variant	1295	-	-	-	-	rs786204227	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,3_prime_UTR_variant	1044	-	-	-	-	rs786204227	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,3_prime_UTR_variant	1117	-	-	-	-	rs786204227	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant,splice_region_variant	984	625	209	H/Y	Cac/Tac	rs786204227	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant,splice_region_variant	1238	985	329	H/Y	Cac/Tac	rs786204227	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant,splice_region_variant	1292	985	329	H/Y	Cac/Tac	rs786204227	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,3_prime_UTR_variant	1368	-	-	-	-	rs786204227	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
188342	17:7669689-7669689	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs786204227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	1243	1101	367	S	agC/agT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,3_prime_UTR_variant	1367	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	1237	1101	367	S	agC/agT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,3_prime_UTR_variant	1294	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,3_prime_UTR_variant	1043	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,synonymous_variant	983	705	235	S	agC/agT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4836;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3845;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,3_prime_UTR_variant	1116	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4527;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4564;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant,splice_region_variant	54	55	19	P/S	Cca/Tca	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,synonymous_variant	1351	984	328	S	agC/agT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,3_prime_UTR_variant	1294	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,3_prime_UTR_variant	1043	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,3_prime_UTR_variant	1116	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,synonymous_variant	983	624	208	S	agC/agT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,synonymous_variant	1237	984	328	S	agC/agT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,synonymous_variant	1291	984	328	S	agC/agT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,3_prime_UTR_variant	1367	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=12/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1792483	17:7669690-7669690	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4825;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3834;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4516;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4553;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000576024.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116590	17:7669697-7669701	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1597345861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597345861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597345861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4829;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597345861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3838;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597345861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4520;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597345861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4557;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000576024.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597345861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
764087	17:7669697-7669697	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1597345861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4828;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3837;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4519;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4556;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000576024.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121207	17:7669698-7669698	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs897689379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs897689379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs897689379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4823;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs897689379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3832;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs897689379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4514;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs897689379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4551;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000576024.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs897689379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918307	17:7669703-7669703	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs897689379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4821;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3830;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4512;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000576024.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1538603	17:7669705-7669705	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4819;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3828;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4510;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000576024.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1620715	17:7669707-7669707	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4787;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3796;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4478;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4515;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269578	17:7669739-7669739	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs17881850,COSV52765252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=4615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3624;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4306;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=4343;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1269356	17:7669911-7669911	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs6503048,COSV53538708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4651;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3948;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4538;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2957;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3639;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3676;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4584;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697674	17:7670578-7670578	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4650;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3947;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4537;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2956;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3638;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3675;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4583;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
810938	17:7670579-7670579	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs17880847,COSV53152345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4634;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3931;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4521;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2940;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3622;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4567;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
514156	17:7670588-7670595	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555524330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4640;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3937;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4527;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2946;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3628;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3665;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4573;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924682	17:7670589-7670589	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2072902431	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4636;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3933;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4523;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2942;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3624;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4569;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387112	17:7670593-7670593	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1056928992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4635;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3932;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4522;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2941;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3623;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4568;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492571	17:7670594-7670594	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555524333	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4634;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3931;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4521;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2940;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3622;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4567;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1558925	17:7670595-7670595	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4632;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3929;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4519;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2938;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3620;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3657;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4565;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
631104	17:7670597-7670597	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567541617	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4630;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3927;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4517;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2936;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3618;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4563;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414032	17:7670599-7670599	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4630;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3927;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4517;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2936;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3618;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4563;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458517	17:7670599-7670599	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs374041625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4629;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3926;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4516;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2935;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3617;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3654;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4562;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1120854	17:7670600-7670600	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1431720273	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4627;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3924;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4514;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2933;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3615;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3652;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4560;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528274	17:7670602-7670602	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs777374791,COSV52761637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1057521454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057521454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057521454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4623;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057521454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3920;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057521454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4510;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057521454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2929;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057521454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3611;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057521454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1057521454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057521454	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4556;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=11/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
382777	17:7670606-7670606	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1057521454	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1237	1095	365	H	caC/caT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1361	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1231	1095	365	H	caC/caT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1288	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4615;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1037	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	977	699	233	H	caC/caT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3912;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4502;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2921;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1110	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3603;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3640;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4548;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1345	978	326	H	caC/caT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1288	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1037	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1110	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	977	618	206	H	caC/caT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1231	978	326	H	caC/caT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1285	978	326	H	caC/caT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1361	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121868	17:7670614-7670614	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1238	978	326	H	caC/caT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1231	1089	363	R	agG/agA	rs1597348743	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1355	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1225	1089	363	R	agG/agA	rs1597348743	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1282	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4609;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1031	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	971	693	231	R	agG/agA	rs1597348743	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3906;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4496;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2915;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1104	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3597;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3634;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4542;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1339	972	324	R	agG/agA	rs1597348743	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1282	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1031	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1104	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	971	612	204	R	agG/agA	rs1597348743	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1225	972	324	R	agG/agA	rs1597348743	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1279	972	324	R	agG/agA	rs1597348743	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1355	-	-	-	-	rs1597348743	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818357	17:7670620-7670620	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1232	972	324	R	agG/agA	rs1597348743	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1225	1083	361	G	ggG/ggA	rs886038349,COSV53093481	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1349	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1219	1083	361	G	ggG/ggA	rs886038349,COSV53093481	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1276	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4603;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1025	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	965	687	229	G	ggG/ggA	rs886038349,COSV53093481	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3900;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4490;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2909;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1098	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3591;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3628;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4536;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1333	966	322	G	ggG/ggA	rs886038349,COSV53093481	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1276	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1025	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1098	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	965	606	202	G	ggG/ggA	rs886038349,COSV53093481	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1219	966	322	G	ggG/ggA	rs886038349,COSV53093481	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1273	966	322	G	ggG/ggA	rs886038349,COSV53093481	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1349	-	-	-	-	rs886038349,COSV53093481	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
256601	17:7670626-7670626	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1226	966	322	G	ggG/ggA	rs886038349,COSV53093481	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1222	1080	360	G	ggG/ggC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1346	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1216	1080	360	G	ggG/ggC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1273	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4600;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1022	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	962	684	228	G	ggG/ggC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3897;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4487;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2906;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1095	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3588;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3625;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4533;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1330	963	321	G	ggG/ggC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1273	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1022	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1095	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	962	603	201	G	ggG/ggC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1216	963	321	G	ggG/ggC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1270	963	321	G	ggG/ggC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1346	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1573907	17:7670629-7670629	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1223	963	321	G	ggG/ggC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1219	1077	359	P	ccA/ccG	rs539224556	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1343	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1213	1077	359	P	ccA/ccG	rs539224556	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1270	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4597;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1019	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	959	681	227	P	ccA/ccG	rs539224556	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3894;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4484;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2903;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1092	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3585;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3622;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4530;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1327	960	320	P	ccA/ccG	rs539224556	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1270	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1019	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1092	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	959	600	200	P	ccA/ccG	rs539224556	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1213	960	320	P	ccA/ccG	rs539224556	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1267	960	320	P	ccA/ccG	rs539224556	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1343	-	-	-	-	rs539224556	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492570	17:7670632-7670632	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1220	960	320	P	ccA/ccG	rs539224556	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1208	1066	356	G/R	Ggg/Cgg	rs766786605,COSV52676335,COSV53210128	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1332	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1202	1066	356	G/R	Ggg/Cgg	rs766786605,COSV52676335,COSV53210128	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1259	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4586;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1008	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	948	670	224	G/R	Ggg/Cgg	rs766786605,COSV52676335,COSV53210128	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3883;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4473;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2892;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1081	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3574;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3611;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4519;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1316	949	317	G/R	Ggg/Cgg	rs766786605,COSV52676335,COSV53210128	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1259	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1008	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1081	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	948	589	197	G/R	Ggg/Cgg	rs766786605,COSV52676335,COSV53210128	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1202	949	317	G/R	Ggg/Cgg	rs766786605,COSV52676335,COSV53210128	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1256	949	317	G/R	Ggg/Cgg	rs766786605,COSV52676335,COSV53210128	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1332	-	-	-	-	rs766786605,COSV52676335,COSV53210128	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
234059	17:7670643-7670643	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1209	949	317	G/R	Ggg/Cgg	rs766786605,COSV52676335,COSV53210128	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1207	1065	355	A	gcT/gcC	rs1057523467	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1331	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1201	1065	355	A	gcT/gcC	rs1057523467	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1258	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4585;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1007	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	947	669	223	A	gcT/gcC	rs1057523467	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3882;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4472;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2891;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1080	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3573;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3610;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4518;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1315	948	316	A	gcT/gcC	rs1057523467	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1258	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1007	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1080	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	947	588	196	A	gcT/gcC	rs1057523467	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1201	948	316	A	gcT/gcC	rs1057523467	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1255	948	316	A	gcT/gcC	rs1057523467	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1331	-	-	-	-	rs1057523467	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
389554	17:7670644-7670644	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1208	948	316	A	gcT/gcC	rs1057523467	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1205	1063	355	A/T	Gct/Act	rs1157427821,COSV52767242	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1329	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1199	1063	355	A/T	Gct/Act	rs1157427821,COSV52767242	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1256	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4583;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1005	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	945	667	223	A/T	Gct/Act	rs1157427821,COSV52767242	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3880;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4470;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2889;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1078	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3571;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3608;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4516;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1313	946	316	A/T	Gct/Act	rs1157427821,COSV52767242	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1256	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1005	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1078	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	945	586	196	A/T	Gct/Act	rs1157427821,COSV52767242	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1199	946	316	A/T	Gct/Act	rs1157427821,COSV52767242	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1253	946	316	A/T	Gct/Act	rs1157427821,COSV52767242	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1329	-	-	-	-	rs1157427821,COSV52767242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1781085	17:7670646-7670646	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1206	946	316	A/T	Gct/Act	rs1157427821,COSV52767242	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1204	1062	354	Q	caG/caA	rs1382535379,COSV53642709	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1328	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1198	1062	354	Q	caG/caA	rs1382535379,COSV53642709	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1255	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4582;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1004	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	944	666	222	Q	caG/caA	rs1382535379,COSV53642709	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3879;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4469;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2888;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1077	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3570;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3607;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4515;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1312	945	315	Q	caG/caA	rs1382535379,COSV53642709	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1255	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1004	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1077	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	944	585	195	Q	caG/caA	rs1382535379,COSV53642709	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1198	945	315	Q	caG/caA	rs1382535379,COSV53642709	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1252	945	315	Q	caG/caA	rs1382535379,COSV53642709	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1328	-	-	-	-	rs1382535379,COSV53642709	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482215	17:7670647-7670647	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1205	945	315	Q	caG/caA	rs1382535379,COSV53642709	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1201	1059	353	A	gcC/gcA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1325	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1195	1059	353	A	gcC/gcA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1252	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4579;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	1001	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	941	663	221	A	gcC/gcA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3876;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4466;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2885;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1074	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3567;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3604;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4512;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1309	942	314	A	gcC/gcA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1252	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	1001	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1074	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	941	582	194	A	gcC/gcA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1195	942	314	A	gcC/gcA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1249	942	314	A	gcC/gcA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1325	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779403	17:7670650-7670650	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1202	942	314	A	gcC/gcA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1198	1056	352	D/E	gaT/gaG	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1322	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1192	1056	352	D/E	gaT/gaG	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1249	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4576;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	998	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	938	660	220	D/E	gaT/gaG	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3873;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4463;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2882;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1071	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3564;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3601;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4509;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1306	939	313	D/E	gaT/gaG	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1249	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	998	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1071	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	938	579	193	D/E	gaT/gaG	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1192	939	313	D/E	gaT/gaG	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1246	939	313	D/E	gaT/gaG	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1322	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1778759	17:7670653-7670653	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1199	939	313	D/E	gaT/gaG	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1192	1050	350	L	ctC/ctT	COSV52954620,COSV53326643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1316	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1186	1050	350	L	ctC/ctT	COSV52954620,COSV53326643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1243	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4570;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	992	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	932	654	218	L	ctC/ctT	COSV52954620,COSV53326643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3867;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4457;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2876;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1065	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3558;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3595;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4503;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1300	933	311	L	ctC/ctT	COSV52954620,COSV53326643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1243	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	992	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1065	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	932	573	191	L	ctC/ctT	COSV52954620,COSV53326643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1186	933	311	L	ctC/ctT	COSV52954620,COSV53326643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1240	933	311	L	ctC/ctT	COSV52954620,COSV53326643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1316	-	-	-	-	COSV52954620,COSV53326643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1776955	17:7670659-7670659	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1193	933	311	L	ctC/ctT	COSV52954620,COSV53326643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1188	1046	349	E/G	gAa/gGa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1312	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1182	1046	349	E/G	gAa/gGa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1239	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4566;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	988	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	928	650	217	E/G	gAa/gGa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3863;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4453;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2872;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1061	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3554;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3591;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4499;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1296	929	310	E/G	gAa/gGa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1239	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	988	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1061	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	928	569	190	E/G	gAa/gGa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1182	929	310	E/G	gAa/gGa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1236	929	310	E/G	gAa/gGa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1312	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1775423	17:7670663-7670663	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1189	929	310	E/G	gAa/gGa	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1183	1041	347	A	gcC/gcT	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1307	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1177	1041	347	A	gcC/gcT	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1234	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4561;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	983	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	923	645	215	A	gcC/gcT	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4448;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2867;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1056	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3549;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3586;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4494;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1291	924	308	A	gcC/gcT	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1234	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	983	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1056	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	923	564	188	A	gcC/gcT	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1177	924	308	A	gcC/gcT	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1231	924	308	A	gcC/gcT	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1307	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1116648	17:7670668-7670668	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1184	924	308	A	gcC/gcT	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1183	1041	347	A	gcC/gcG	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1307	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1177	1041	347	A	gcC/gcG	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1234	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4561;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	983	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	923	645	215	A	gcC/gcG	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4448;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2867;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1056	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3549;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3586;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4494;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1291	924	308	A	gcC/gcG	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1234	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	983	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1056	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	923	564	188	A	gcC/gcG	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1177	924	308	A	gcC/gcG	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1231	924	308	A	gcC/gcG	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1307	-	-	-	-	rs1450229137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486998	17:7670668-7670668	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1184	924	308	A	gcC/gcG	rs1450229137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1180	1038	346	E	gaG/gaA	rs1555524406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1304	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1174	1038	346	E	gaG/gaA	rs1555524406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1231	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4558;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	980	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	920	642	214	E	gaG/gaA	rs1555524406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3855;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4445;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2864;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1053	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3546;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3583;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4491;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1288	921	307	E	gaG/gaA	rs1555524406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1231	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	980	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1053	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	920	561	187	E	gaG/gaA	rs1555524406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1174	921	307	E	gaG/gaA	rs1555524406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1228	921	307	E	gaG/gaA	rs1555524406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1304	-	-	-	-	rs1555524406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482222	17:7670671-7670671	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1181	921	307	E	gaG/gaA	rs1555524406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1174	1032	344	L	ctG/ctA	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1298	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1168	1032	344	L	ctG/ctA	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1225	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4552;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	974	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	914	636	212	L	ctG/ctA	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3849;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4439;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2858;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1047	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3540;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3577;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4485;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1282	915	305	L	ctG/ctA	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1225	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	974	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1047	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	914	555	185	L	ctG/ctA	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1168	915	305	L	ctG/ctA	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1222	915	305	L	ctG/ctA	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1298	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
220903	17:7670677-7670677	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1175	915	305	L	ctG/ctA	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1174	1032	344	L	ctG/ctC	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1298	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1168	1032	344	L	ctG/ctC	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1225	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4552;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	974	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	914	636	212	L	ctG/ctC	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3849;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4439;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2858;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1047	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3540;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3577;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4485;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1282	915	305	L	ctG/ctC	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1225	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	974	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1047	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	914	555	185	L	ctG/ctC	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1168	915	305	L	ctG/ctC	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1222	915	305	L	ctG/ctC	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1298	-	-	-	-	rs752189180,COSV53388115,COSV53846847	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458512	17:7670677-7670677	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1175	915	305	L	ctG/ctC	rs752189180,COSV53388115,COSV53846847	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1172	1030	344	L	Ctg/Ttg	rs1597349242	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1296	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1166	1030	344	L	Ctg/Ttg	rs1597349242	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1223	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4550;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	972	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	912	634	212	L	Ctg/Ttg	rs1597349242	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3847;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4437;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2856;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1045	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3538;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3575;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4483;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1280	913	305	L	Ctg/Ttg	rs1597349242	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1223	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	972	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1045	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	912	553	185	L	Ctg/Ttg	rs1597349242	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1166	913	305	L	Ctg/Ttg	rs1597349242	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1220	913	305	L	Ctg/Ttg	rs1597349242	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1296	-	-	-	-	rs1597349242	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
818289	17:7670679-7670679	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1173	913	305	L	Ctg/Ttg	rs1597349242	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1168	1026	342	R	cgA/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1292	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1162	1026	342	R	cgA/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1219	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4546;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	968	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	908	630	210	R	cgA/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3843;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4433;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2852;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1041	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3534;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3571;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4479;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1276	909	303	R	cgA/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1219	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	968	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1041	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	908	549	183	R	cgA/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1162	909	303	R	cgA/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1216	909	303	R	cgA/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1292	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1158153	17:7670683-7670683	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1169	909	303	R	cgA/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1165	1023	341	F	ttC/ttT	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1289	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1159	1023	341	F	ttC/ttT	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1216	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4543;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	965	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	905	627	209	F	ttC/ttT	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3840;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4430;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2849;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1038	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3531;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3568;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4476;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1273	906	302	F	ttC/ttT	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1216	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	965	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1038	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	905	546	182	F	ttC/ttT	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1159	906	302	F	ttC/ttT	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1213	906	302	F	ttC/ttT	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1289	-	-	-	-	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220073	17:7670686-7670686	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1166	906	302	F	ttC/ttT	rs864622369,COSV52693704,COSV52845855,COSV99411018	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1162	1020	340	M/I	atG/atT	rs1463722976,COSV52784428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1286	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1156	1020	340	M/I	atG/atT	rs1463722976,COSV52784428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1213	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4540;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	962	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	902	624	208	M/I	atG/atT	rs1463722976,COSV52784428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3837;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4427;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2846;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1035	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3528;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3565;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4473;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1270	903	301	M/I	atG/atT	rs1463722976,COSV52784428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1213	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	962	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1035	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	902	543	181	M/I	atG/atT	rs1463722976,COSV52784428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1156	903	301	M/I	atG/atT	rs1463722976,COSV52784428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1210	903	301	M/I	atG/atT	rs1463722976,COSV52784428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1286	-	-	-	-	rs1463722976,COSV52784428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
1759327	17:7670689-7670689	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1163	903	301	M/I	atG/atT	rs1463722976,COSV52784428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1156	1014	338	F	ttC/ttT	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1280	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1150	1014	338	F	ttC/ttT	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1207	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4534;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	956	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	896	618	206	F	ttC/ttT	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3831;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4421;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2840;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1029	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3522;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3559;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4467;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1264	897	299	F	ttC/ttT	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1207	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	956	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1029	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	896	537	179	F	ttC/ttT	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1150	897	299	F	ttC/ttT	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1204	897	299	F	ttC/ttT	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1280	-	-	-	-	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
182952	17:7670695-7670695	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1157	897	299	F	ttC/ttT	rs150293825,COSV52857417,COSV52875604,COSV52988223	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1153	1011	337	R	cgC/cgT	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1277	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1147	1011	337	R	cgC/cgT	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1204	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4531;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	953	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	893	615	205	R	cgC/cgT	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3828;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4418;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2837;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1026	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3519;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3556;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4464;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1261	894	298	R	cgC/cgT	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1204	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	953	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1026	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	893	534	178	R	cgC/cgT	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1147	894	298	R	cgC/cgT	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1201	894	298	R	cgC/cgT	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1277	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
512946	17:7670698-7670698	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1154	894	298	R	cgC/cgT	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1153	1011	337	R	cgC/cgG	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1277	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1147	1011	337	R	cgC/cgG	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1204	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4531;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	953	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	893	615	205	R	cgC/cgG	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3828;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4418;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2837;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1026	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3519;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3556;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4464;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1261	894	298	R	cgC/cgG	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1204	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	953	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1026	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	893	534	178	R	cgC/cgG	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1147	894	298	R	cgC/cgG	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1201	894	298	R	cgC/cgG	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1277	-	-	-	-	rs1218459955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
633018	17:7670698-7670698	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1154	894	298	R	cgC/cgG	rs1218459955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1150	1008	336	E	gaG/gaA	rs1555524453,COSV105878400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1274	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1144	1008	336	E	gaG/gaA	rs1555524453,COSV105878400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1201	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4528;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	950	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	890	612	204	E	gaG/gaA	rs1555524453,COSV105878400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3825;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4415;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2834;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1023	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3516;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3553;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4461;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1258	891	297	E	gaG/gaA	rs1555524453,COSV105878400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1201	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	950	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1023	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	890	531	177	E	gaG/gaA	rs1555524453,COSV105878400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1144	891	297	E	gaG/gaA	rs1555524453,COSV105878400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1198	891	297	E	gaG/gaA	rs1555524453,COSV105878400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1274	-	-	-	-	rs1555524453,COSV105878400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482236	17:7670701-7670701	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1151	891	297	E	gaG/gaA	rs1555524453,COSV105878400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1147	1005	335	R	cgT/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1271	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1141	1005	335	R	cgT/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1198	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4525;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	947	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	887	609	203	R	cgT/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3822;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4412;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2831;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1020	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3513;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4458;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1255	888	296	R	cgT/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1198	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	947	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1020	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	887	528	176	R	cgT/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1141	888	296	R	cgT/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1195	888	296	R	cgT/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1271	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086350	17:7670704-7670704	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1148	888	296	R	cgT/cgG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1144	1002	334	G	ggG/ggA	rs786203531,COSV99439495	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1268	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1138	1002	334	G	ggG/ggA	rs786203531,COSV99439495	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1195	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4522;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	944	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	884	606	202	G	ggG/ggA	rs786203531,COSV99439495	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3819;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4409;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2828;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1017	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3510;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3547;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4455;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1252	885	295	G	ggG/ggA	rs786203531,COSV99439495	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1195	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	944	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1017	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	884	525	175	G	ggG/ggA	rs786203531,COSV99439495	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1138	885	295	G	ggG/ggA	rs786203531,COSV99439495	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1192	885	295	G	ggG/ggA	rs786203531,COSV99439495	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1268	-	-	-	-	rs786203531,COSV99439495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187180	17:7670707-7670707	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1145	885	295	G	ggG/ggA	rs786203531,COSV99439495	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1140	998	333	R/H	cGt/cAt	rs573154688,COSV52748025,COSV52990800	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1264	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1134	998	333	R/H	cGt/cAt	rs573154688,COSV52748025,COSV52990800	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1191	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4518;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	940	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	880	602	201	R/H	cGt/cAt	rs573154688,COSV52748025,COSV52990800	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3815;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4405;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2824;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1013	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3506;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3543;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4451;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1248	881	294	R/H	cGt/cAt	rs573154688,COSV52748025,COSV52990800	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1191	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	940	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1013	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	880	521	174	R/H	cGt/cAt	rs573154688,COSV52748025,COSV52990800	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1134	881	294	R/H	cGt/cAt	rs573154688,COSV52748025,COSV52990800	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1188	881	294	R/H	cGt/cAt	rs573154688,COSV52748025,COSV52990800	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1264	-	-	-	-	rs573154688,COSV52748025,COSV52990800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
142273	17:7670711-7670711	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1141	881	294	R/H	cGt/cAt	rs573154688,COSV52748025,COSV52990800	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1139	997	333	R/C	Cgt/Tgt	rs769934890,CM137619,COSV52774724	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1263	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1133	997	333	R/C	Cgt/Tgt	rs769934890,CM137619,COSV52774724	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1190	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4517;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	939	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	879	601	201	R/C	Cgt/Tgt	rs769934890,CM137619,COSV52774724	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3814;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4404;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2823;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	1012	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3505;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3542;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4450;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1247	880	294	R/C	Cgt/Tgt	rs769934890,CM137619,COSV52774724	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1190	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	939	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	1012	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	879	520	174	R/C	Cgt/Tgt	rs769934890,CM137619,COSV52774724	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1133	880	294	R/C	Cgt/Tgt	rs769934890,CM137619,COSV52774724	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1187	880	294	R/C	Cgt/Tgt	rs769934890,CM137619,COSV52774724	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1263	-	-	-	-	rs769934890,CM137619,COSV52774724	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
184745	17:7670712-7670712	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1140	880	294	R/C	Cgt/Tgt	rs769934890,CM137619,COSV52774724	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	1138	996	332	I	atC/atT	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,3_prime_UTR_variant	1262	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	1132	996	332	I	atC/atT	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,3_prime_UTR_variant	1189	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4516;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,3_prime_UTR_variant	938	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,synonymous_variant	878	600	200	I	atC/atT	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3813;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4403;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2822;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,3_prime_UTR_variant	1011	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3504;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3541;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4449;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,synonymous_variant	1246	879	293	I	atC/atT	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,3_prime_UTR_variant	1189	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,3_prime_UTR_variant	938	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,3_prime_UTR_variant	1011	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,synonymous_variant	878	519	173	I	atC/atT	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,synonymous_variant	1132	879	293	I	atC/atT	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,synonymous_variant	1186	879	293	I	atC/atT	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,3_prime_UTR_variant	1262	-	-	-	-	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=11/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
798976	17:7670713-7670713	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,synonymous_variant,NMD_transcript_variant	1139	879	293	I	atC/atT	rs1555524470,CM121765,COSV52683770,COSV52736313	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4508;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3805;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4395;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2814;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3496;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4441;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540067	17:7670720-7670720	CC	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs375273756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs375273756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs375273756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4509;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375273756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3806;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375273756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4396;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375273756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2815;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375273756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3497;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs375273756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3534;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs375273756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375273756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4442;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458581	17:7670720-7670720	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs375273756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4508;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3805;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4395;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2814;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3496;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4441;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1079313	17:7670721-7670721	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4508;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3805;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4395;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2814;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3496;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4441;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540068	17:7670721-7670721	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555524474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4508;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3805;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4395;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2814;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3496;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1555524474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4441;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458582	17:7670721-7670721	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555524474	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV53222948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV53222948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53222948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4506;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53222948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3803;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53222948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4393;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53222948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2812;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53222948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3494;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53222948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3531;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	COSV53222948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53222948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4439;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1122992	17:7670723-7670723	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	COSV53222948	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4504;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3801;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4391;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2810;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3492;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3529;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4437;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105087	17:7670725-7670725	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1057522329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057522329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4502;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3799;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4389;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2808;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3490;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3527;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1057522329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522329	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4435;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385783	17:7670727-7670727	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1057522329	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4497;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3794;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4384;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2803;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3485;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4430;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552196	17:7670732-7670732	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4497;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3794;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4384;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2803;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3485;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4430;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802904	17:7670732-7670732	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs368691910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs368691910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs368691910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4497;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs368691910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=3794;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs368691910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4384;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs368691910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2803;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs368691910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3485;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs368691910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=3522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs368691910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs368691910	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4430;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182951	17:7670732-7670732	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs368691910	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2271;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1568;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2158;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=577;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1259;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1296;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2204;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1288516	17:7672958-7672958	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs60699444,COSV104370780,COSV53140096	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1,1;PHENO=1,1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2199;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1496;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2086;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=505;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1187;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1224;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2132;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1237084	17:7673030-7673030	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs75732100,COSV104369765	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2103;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1400;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1990;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=409;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1091;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1128;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2036;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1250065	17:7673125-7673125	AA	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2103;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1400;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1990;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=409;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1091;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1128;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2036;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1259818	17:7673125-7673126	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs34308401	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2046;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1343;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1933;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=352;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1034;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1071;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1979;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1246968	17:7673183-7673183	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs77697176,COSV104581685	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,3_prime_UTR_variant,intron_variant	1257-?	-	-	-	-	rs730882013	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_variant,splice_donor_5th_base_variant,3_prime_UTR_variant,intron_variant	1184-?	-	-	-	-	rs730882013	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2020;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,3_prime_UTR_variant,intron_variant	933-?	-	-	-	-	rs730882013	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1317;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1907;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=326;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_variant,splice_donor_5th_base_variant,3_prime_UTR_variant,intron_variant	1006-?	-	-	-	-	rs730882013	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1008;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1045;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1953;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,3_prime_UTR_variant,intron_variant	1184-?	-	-	-	-	rs730882013	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,3_prime_UTR_variant,intron_variant	933-?	-	-	-	-	rs730882013	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,3_prime_UTR_variant,intron_variant	1006-?	-	-	-	-	rs730882013	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_variant,splice_donor_5th_base_variant,3_prime_UTR_variant,intron_variant	1257-?	-	-	-	-	rs730882013	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182950	17:7673193-7673209	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs730882013	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=benign,likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1438885967	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1438885967	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2025;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1438885967	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1322;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1912;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=331;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1438885967	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1013;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1050;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1958;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1438885967	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1438885967	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1438885967	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1438885967	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628372	17:7673204-7673204	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1438885967	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs772238542	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs772238542	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2024;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs772238542	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1321;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1911;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=330;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs772238542	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1012;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1049;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1957;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs772238542	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs772238542	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs772238542	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs772238542	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=10/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
927924	17:7673204-7673204	AAG	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs772238542	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;PHENO=1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1249	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1176	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2012;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	925	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1309;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1899;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=318;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	998	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1000;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1037;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1945;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1176	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	925	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	998	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1249	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
631028	17:7673217-7673217	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567545196,COSV104370823,COSV53534010	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1248	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000455263.6	Transcript	3_prime_UTR_variant	1175	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2011;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000504290.5	Transcript	3_prime_UTR_variant	924	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1308;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1898;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=317;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	997	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=999;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1036;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1944;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000610538.4	Transcript	3_prime_UTR_variant	1175	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000610623.4	Transcript	3_prime_UTR_variant	924	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	997	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1248	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
627761	17:7673218-7673218	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1245315319,COSV99477373	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1243-1245	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000455263.6	Transcript	inframe_deletion	1170-1172	1037-1039	346-347	S*/*	tCGTaa/taa	rs1555524872	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2006;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000504290.5	Transcript	inframe_deletion	919-921	641-643	214-215	S*/*	tCGTaa/taa	rs1555524872	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1303;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1893;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=312;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	992-994	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=994;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1031;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1939;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000610538.4	Transcript	inframe_deletion	1170-1172	920-922	307-308	S*/*	tCGTaa/taa	rs1555524872	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000610623.4	Transcript	inframe_deletion	919-921	560-562	187-188	S*/*	tCGTaa/taa	rs1555524872	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	992-994	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1243-1245	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
548873	17:7673220-7673223	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555524872	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1245-1246	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000455263.6	Transcript	frameshift_variant,stop_lost	1172-1173	1039-1040	347	*/LX	taa/tTaa	rs1567545210	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2008;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000504290.5	Transcript	frameshift_variant,stop_lost	921-922	643-644	215	*/LX	taa/tTaa	rs1567545210	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1305;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1895;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=314;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	994-995	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=996;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1033;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1941;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000610538.4	Transcript	frameshift_variant,stop_lost	1172-1173	922-923	308	*/LX	taa/tTaa	rs1567545210	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000610623.4	Transcript	frameshift_variant,stop_lost	921-922	562-563	188	*/LX	taa/tTaa	rs1567545210	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	994-995	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1245-1246	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627874	17:7673220-7673220	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567545210	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1244	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1171	1038	346	S	tcG/tcA	rs372821099	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2007;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	920	642	214	S	tcG/tcA	rs372821099	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1304;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1894;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=313;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	993	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=995;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1032;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1940;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1171	921	307	S	tcG/tcA	rs372821099	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	920	561	187	S	tcG/tcA	rs372821099	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	993	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1244	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492651	17:7673222-7673222	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs372821099	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1243	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1170	1037	346	S/L	tCg/tTg	rs756952434,COSV52819048,COSV52956881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2006;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	919	641	214	S/L	tCg/tTg	rs756952434,COSV52819048,COSV52956881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1303;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1893;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=312;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	992	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=994;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1031;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1939;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1170	920	307	S/L	tCg/tTg	rs756952434,COSV52819048,COSV52956881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	919	560	187	S/L	tCg/tTg	rs756952434,COSV52819048,COSV52956881	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	992	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1243	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492650	17:7673223-7673223	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs756952434,COSV52819048,COSV52956881	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1241	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1168	1035	345	S	tcG/tcA	rs201293647,COSV53840378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2004;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	917	639	213	S	tcG/tcA	rs201293647,COSV53840378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1301;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1891;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=310;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	990	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=992;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1029;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1937;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1168	918	306	S	tcG/tcA	rs201293647,COSV53840378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	917	558	186	S	tcG/tcA	rs201293647,COSV53840378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	990	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1241	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492649	17:7673225-7673225	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1241	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1168	1035	345	S	tcG/tcT	rs201293647,COSV53840378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2004;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	917	639	213	S	tcG/tcT	rs201293647,COSV53840378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1301;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1891;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=310;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	990	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=992;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1029;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1937;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1168	918	306	S	tcG/tcT	rs201293647,COSV53840378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	917	558	186	S	tcG/tcT	rs201293647,COSV53840378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	990	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1241	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629929	17:7673225-7673225	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs201293647,COSV53840378	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1238	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1165	1032	344	N/K	aaC/aaG	rs200274944,COSV106055877	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2001;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	914	636	212	N/K	aaC/aaG	rs200274944,COSV106055877	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1298;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1888;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=307;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	987	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=989;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1026;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1934;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1165	915	305	N/K	aaC/aaG	rs200274944,COSV106055877	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	914	555	185	N/K	aaC/aaG	rs200274944,COSV106055877	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	987	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1238	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492647	17:7673228-7673228	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs200274944,COSV106055877	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1230	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1157	1024	342	L	Ctg/Ttg	rs770028766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1993;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	906	628	210	L	Ctg/Ttg	rs770028766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1290;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1880;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=299;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	979	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=981;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1018;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1926;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1157	907	303	L	Ctg/Ttg	rs770028766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	906	547	183	L	Ctg/Ttg	rs770028766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	979	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1230	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927925	17:7673236-7673236	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs770028766	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1226	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1153	1020	340	Y	taC/taT	rs1351357911,COSV104584367	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1989;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	902	624	208	Y	taC/taT	rs1351357911,COSV104584367	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1286;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1876;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=295;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	975	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=977;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1014;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1922;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1153	903	301	Y	taC/taT	rs1351357911,COSV104584367	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	902	543	181	Y	taC/taT	rs1351357911,COSV104584367	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	975	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1226	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920212	17:7673240-7673240	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1351357911,COSV104584367	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1221	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1148	1015	339	C/R	Tgt/Cgt	rs1642789	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1984;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	897	619	207	C/R	Tgt/Cgt	rs1642789	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1281;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1871;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=290;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	970	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=972;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1009;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1917;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1148	898	300	C/R	Tgt/Cgt	rs1642789	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	897	538	180	C/R	Tgt/Cgt	rs1642789	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	970	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1221	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492646	17:7673245-7673245	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1642789	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1220	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000455263.6	Transcript	stop_gained	1147	1014	338	W/*	tgG/tgA	rs1337983762	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1983;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000504290.5	Transcript	stop_gained	896	618	206	W/*	tgG/tgA	rs1337983762	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1280;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1870;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=289;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	969	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1008;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1916;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000610538.4	Transcript	stop_gained	1147	897	299	W/*	tgG/tgA	rs1337983762	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000610623.4	Transcript	stop_gained	896	537	179	W/*	tgG/tgA	rs1337983762	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	969	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1220	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630847	17:7673246-7673246	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1337983762	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1218	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1145	1012	338	W/R	Tgg/Cgg	rs749361930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1981;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	894	616	206	W/R	Tgg/Cgg	rs749361930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1278;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1868;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=287;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	967	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=969;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1006;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1914;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1145	895	299	W/R	Tgg/Cgg	rs749361930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	894	535	179	W/R	Tgg/Cgg	rs749361930	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	967	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1218	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492645	17:7673248-7673248	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs749361930	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1217	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1144	1011	337	R	cgA/cgG	rs1270269782	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1980;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	893	615	205	R	cgA/cgG	rs1270269782	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1277;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1867;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=286;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	966	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=968;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1005;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1913;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1144	894	298	R	cgA/cgG	rs1270269782	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	893	534	178	R	cgA/cgG	rs1270269782	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	966	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1217	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924881	17:7673249-7673249	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1270269782	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1216	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1143	1010	337	R/Q	cGa/cAa	rs771319678,COSV104586061	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1979;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	892	614	205	R/Q	cGa/cAa	rs771319678,COSV104586061	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1276;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1866;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=285;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	965	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=967;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1004;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1912;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1143	893	298	R/Q	cGa/cAa	rs771319678,COSV104586061	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	892	533	178	R/Q	cGa/cAa	rs771319678,COSV104586061	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	965	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1216	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492644	17:7673250-7673250	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs771319678,COSV104586061	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1208	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1135	1002	334	L	ctT/ctA	rs2073120784	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1971;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	884	606	202	L	ctT/ctA	rs2073120784	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1268;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1858;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=277;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	957	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=959;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=996;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1904;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1135	885	295	L	ctT/ctA	rs2073120784	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	884	525	175	L	ctT/ctA	rs2073120784	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	957	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1208	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920392	17:7673258-7673258	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2073120784	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1198	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs2073121951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1961;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs2073121951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1258;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1848;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=267;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	947	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=949;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=986;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1894;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs2073121951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs2073121951	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	947	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1198	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
926994	17:7673268-7673268	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2073121951	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1188	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1373684374	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1951;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1373684374	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1248;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1838;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=257;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	937	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=939;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=976;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1884;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1373684374	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1373684374	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	937	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1188	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
803306	17:7673277-7673278	-	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1373684374	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1179	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1942;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1239;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1829;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=248;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	928	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=930;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=967;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1875;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	928	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1179	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492642	17:7673287-7673287	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555524889	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1176	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1939;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1236;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1826;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=245;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	925	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=927;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=964;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1872;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	925	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1176	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492641	17:7673290-7673290	T	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs978869607	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1175	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1938;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1235;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1825;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=244;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	924	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=926;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=963;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1871;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	924	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1175	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
371863	17:7673291-7673291	T	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1175	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1938;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1235;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1825;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=244;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	924	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=926;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=963;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1871;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	924	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1175	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492640	17:7673291-7673291	G	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs576532147,COSV52918848	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1171	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1934;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1231;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1821;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=240;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	920	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=922;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=959;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1867;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	920	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1171	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
920442	17:7673295-7673295	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1392806365	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1165	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1928;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1225;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1815;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=234;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	914	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=916;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=953;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1861;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	914	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1165	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
371962	17:7673301-7673301	T	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs17883348	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000420246.6	Transcript	3_prime_UTR_variant	1163	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1926;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1223;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1813;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=232;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000510385.5	Transcript	3_prime_UTR_variant	912	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=914;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=951;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1859;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000618944.4	Transcript	3_prime_UTR_variant	912	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000622645.4	Transcript	3_prime_UTR_variant	1163	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630888	17:7673303-7673303	G	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1470589675,COSV104369764	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000420246.6	Transcript	stop_retained_variant	1159	1026	342	*	taA/taG	rs761121529	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1922;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1219;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1809;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=228;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000510385.5	Transcript	stop_retained_variant	908	630	210	*	taA/taG	rs761121529	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=910;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=947;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1855;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000618944.4	Transcript	stop_retained_variant	908	549	183	*	taA/taG	rs761121529	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000622645.4	Transcript	stop_retained_variant	1159	909	303	*	taA/taG	rs761121529	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492639	17:7673307-7673307	C	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs761121529	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000420246.6	Transcript	stop_lost	1158	1025	342	*/S	tAa/tCa	rs764562217,COSV53125141,COSV53273956	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1921;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1218;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1808;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=227;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000510385.5	Transcript	stop_lost	907	629	210	*/S	tAa/tCa	rs764562217,COSV53125141,COSV53273956	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=909;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=946;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1854;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000618944.4	Transcript	stop_lost	907	548	183	*/S	tAa/tCa	rs764562217,COSV53125141,COSV53273956	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000622645.4	Transcript	stop_lost	1158	908	303	*/S	tAa/tCa	rs764562217,COSV53125141,COSV53273956	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
372008	17:7673308-7673308	G	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs764562217,COSV53125141,COSV53273956	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1154	1021	341	C/G	Tgt/Ggt	rs3021068	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1917;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1214;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1804;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=223;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	903	625	209	C/G	Tgt/Ggt	rs3021068	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=942;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1850;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	903	544	182	C/G	Tgt/Ggt	rs3021068	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1154	904	302	C/G	Tgt/Ggt	rs3021068	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
135361	17:7673312-7673312	C	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=not_provided,benign,likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1154	1021	341	C/R	Tgt/Cgt	rs3021068	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1917;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1214;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1804;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=223;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	903	625	209	C/R	Tgt/Cgt	rs3021068	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=942;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1850;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	903	544	182	C/R	Tgt/Cgt	rs3021068	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1154	904	302	C/R	Tgt/Cgt	rs3021068	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492638	17:7673312-7673312	G	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs3021068	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1147	1014	338	K/N	aaA/aaC	rs761303879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1910;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1207;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1797;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=216;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	896	618	206	K/N	aaA/aaC	rs761303879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=898;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=935;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1843;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	896	537	179	K/N	aaA/aaC	rs761303879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1147	897	299	K/N	aaA/aaC	rs761303879	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492637	17:7673319-7673319	G	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs761303879	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1144	1011	337	Q	caA/caG	rs912136376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1907;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1204;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1794;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=213;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	893	615	205	Q	caA/caG	rs912136376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=932;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1840;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	893	534	178	Q	caA/caG	rs912136376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1144	894	298	Q	caA/caG	rs912136376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492636	17:7673322-7673322	C	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs912136376	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1134	1001	334	T/I	aCc/aTc	rs2073127723,COSV52956891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1897;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1194;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1784;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=203;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	883	605	202	T/I	aCc/aTc	rs2073127723,COSV52956891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=885;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=922;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1830;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	883	524	175	T/I	aCc/aTc	rs2073127723,COSV52956891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1134	884	295	T/I	aCc/aTc	rs2073127723,COSV52956891	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
924895	17:7673332-7673332	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2073127723,COSV52956891	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1130	997	333	Q/E	Cag/Gag	rs764851816	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1893;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1190;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1780;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=199;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	879	601	201	Q/E	Cag/Gag	rs764851816	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=881;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=918;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1826;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	879	520	174	Q/E	Cag/Gag	rs764851816	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1130	880	294	Q/E	Cag/Gag	rs764851816	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492635	17:7673336-7673336	C	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs764851816	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,synonymous_variant	1129	996	332	D	gaC/gaT	rs750031971	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1892;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1189;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1779;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=198;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,synonymous_variant	878	600	200	D	gaC/gaT	rs750031971	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=880;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=917;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1825;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,synonymous_variant	878	519	173	D	gaC/gaT	rs750031971	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,synonymous_variant	1129	879	293	D	gaC/gaT	rs750031971	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=10/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492634	17:7673337-7673337	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs750031971	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_acceptor_variant	-	-	-	-	-	rs2073129357	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1889;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1186;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1776;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=195;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_acceptor_variant	-	-	-	-	-	rs2073129357	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=877;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=914;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1822;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs2073129357	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_acceptor_variant	-	-	-	-	-	rs2073129357	IMPACT=HIGH;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
918568	17:7673340-7673340	T	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2073129357	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs758130745	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1883;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1180;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1770;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=189;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs758130745	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=871;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=908;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1816;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs758130745	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs758130745	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492633	17:7673346-7673346	T	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs758130745	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1883;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1180;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1770;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=189;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs758130745	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=871;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=908;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1816;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs758130745	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs758130745	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
919516	17:7673346-7673346	G	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs758130745	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1362238110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1879;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1176;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1766;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=185;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1362238110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=867;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1812;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1362238110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1362238110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
928139	17:7673350-7673350	C	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1362238110	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073130332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1878;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1175;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1765;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=184;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073130332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=866;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=903;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1811;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073130332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073130332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
927601	17:7673351-7673351	G	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2073130332	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1871;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1168;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1758;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=177;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=896;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1804;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
630681	17:7673358-7673358	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567545538	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1870;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1167;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1757;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=176;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=895;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1803;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
627694	17:7673359-7673359	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs945008591	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1860;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1157;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1747;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=166;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=848;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=885;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1793;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1679015	17:7673368-7673368	GT	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;PHENO=1
1679015	17:7673368-7673368	GT	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs775788764	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;PHENO=1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1835;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1132;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1722;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=141;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=823;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=860;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1768;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
224042	17:7673394-7673394	T	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs371592265,COSV53490606	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1709;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1006;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1596;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=15;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=697;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=734;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1642;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492632	17:7673520-7673520	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555524931	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1708;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1005;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1595;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=733;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1641;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1539108	17:7673521-7673521	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
1539108	17:7673521-7673521	G	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=TF_binding_site
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1706;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1003;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1593;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=12;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=694;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1639;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1540054	17:7673522-7673523	TG	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
1540054	17:7673522-7673523	TG	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=TF_binding_site
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1707;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1004;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1594;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=13;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=695;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=732;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1640;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552614	17:7673522-7673522	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
1552614	17:7673522-7673522	T	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=TF_binding_site
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1706;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1003;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1593;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=12;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=694;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=731;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000576024.1	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1639;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
93325	17:7673523-7673523	G	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1800899,CS1516647,COSV53015717	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=benign/likely_benign,benign,likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1701;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=998;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1588;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000509690.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=7;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=689;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=726;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000576024.1	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/1;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1634;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1557740	17:7673527-7673527	TTAG	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
1557740	17:7673527-7673527	TTAG	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=TF_binding_site
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1126	984	328	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	984	984	328	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057520387,COSV104587912,COSV52729284	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1117	984	328	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1120	984	328	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1117	984	328	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520387,COSV104587912,COSV52729284	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1685;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	866	588	196	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	866	588	196	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520387,COSV104587912,COSV52729284	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520387,COSV104587912,COSV52729284	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1572;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	720	588	196	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	866	588	196	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520387,COSV104587912,COSV52729284	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=673;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520387,COSV104587912,COSV52729284	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=710;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000576024.1	Transcript	synonymous_variant	44	45	15	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520387,COSV104587912,COSV52729284	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1618;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1234	867	289	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1117	867	289	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	866	507	169	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	866	507	169	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	866	507	169	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1120	867	289	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1174	867	289	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1117	867	289	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1127	867	289	F	ttC/ttT	rs1057520387,COSV104587912,COSV52729284	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057520387,COSV104587912,COSV52729284	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
378748	17:7673544-7673544	A	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057520387,COSV104587912,COSV52729284	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1117	975	325	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	975	975	325	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1245012034	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1108	975	325	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1111	975	325	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1108	975	325	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1245012034	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1676;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	857	579	193	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	857	579	193	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1245012034	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=973;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1245012034	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1563;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	711	579	193	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	857	579	193	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1245012034	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=664;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1245012034	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=701;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000576024.1	Transcript	synonymous_variant	35	36	12	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1245012034	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1609;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1225	858	286	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1108	858	286	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	857	498	166	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	857	498	166	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	857	498	166	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1111	858	286	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1165	858	286	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1108	858	286	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1118	858	286	G	ggA/ggG	rs1245012034	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1245012034	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
458578	17:7673553-7673553	C	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1245012034	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1111	969	323	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	969	969	323	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs672601297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1102	969	323	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1105	969	323	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1102	969	323	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs672601297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1670;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	851	573	191	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	851	573	191	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs672601297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=967;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs672601297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1557;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	705	573	191	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	851	573	191	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs672601297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=658;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs672601297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=695;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000576024.1	Transcript	synonymous_variant	29	30	10	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs672601297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1603;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1219	852	284	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1102	852	284	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	851	492	164	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	851	492	164	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	851	492	164	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1105	852	284	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1159	852	284	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1102	852	284	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1112	852	284	L	ctG/ctA	rs672601297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs672601297	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign,not_provided;PHENO=1
132974	17:7673559-7673559	T	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs672601297	IMPACT=MODIFIER;BIOTYPE=TF_binding_site;CLIN_SIG=likely_benign,not_provided;PHENO=1
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1111	969	323	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	969	969	323	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1102	969	323	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1105	969	323	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1102	969	323	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1670;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	851	573	191	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	851	573	191	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=967;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1557;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	705	573	191	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	851	573	191	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=658;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=695;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000576024.1	Transcript	synonymous_variant	29	30	10	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1603;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1219	852	284	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1102	852	284	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	851	492	164	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	851	492	164	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	851	492	164	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1105	852	284	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1159	852	284	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1102	852	284	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1112	852	284	L	ctG/ctC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767853	17:7673559-7673559	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
1767853	17:7673559-7673559	G	-	ENSR00000548581	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=TF_binding_site
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1096	954	318	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	954	954	318	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52837378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1087	954	318	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1090	954	318	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1087	954	318	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52837378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1655;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	836	558	186	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	836	558	186	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52837378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=952;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52837378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1542;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	690	558	186	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	836	558	186	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52837378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=643;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52837378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=680;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000576024.1	Transcript	synonymous_variant	14	15	5	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52837378	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1588;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1204	837	279	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1087	837	279	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	836	477	159	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	836	477	159	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	836	477	159	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1090	837	279	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1144	837	279	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1087	837	279	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1097	837	279	P	ccA/ccG	COSV52837378	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1544418	17:7673574-7673574	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52837378	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1;PHENO=1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1093	951	317	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	951	951	317	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1060501199,CD156962,COSV53738699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1084	951	317	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1087	951	317	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1084	951	317	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501199,CD156962,COSV53738699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1652;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	833	555	185	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	833	555	185	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501199,CD156962,COSV53738699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=949;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501199,CD156962,COSV53738699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1539;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	687	555	185	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	833	555	185	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501199,CD156962,COSV53738699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=640;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501199,CD156962,COSV53738699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=677;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000576024.1	Transcript	synonymous_variant	11	12	4	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501199,CD156962,COSV53738699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1585;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1201	834	278	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1084	834	278	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	833	474	158	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	833	474	158	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	833	474	158	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1087	834	278	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1141	834	278	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1084	834	278	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1094	834	278	Q	caG/caA	rs1060501199,CD156962,COSV53738699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
627965	17:7673577-7673577	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1060501199,CD156962,COSV53738699	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1090	948	316	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	948	948	316	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1081	948	316	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1084	948	316	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1081	948	316	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1649;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	830	552	184	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	830	552	184	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=946;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1536;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	684	552	184	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	830	552	184	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=637;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=674;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000576024.1	Transcript	synonymous_variant	8	9	3	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1582;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1198	831	277	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1081	831	277	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	830	471	157	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	830	471	157	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	830	471	157	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1084	831	277	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1138	831	277	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1081	831	277	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1091	831	277	P	ccC/ccG	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1172210	17:7673580-7673580	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1090	948	316	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	948	948	316	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1081	948	316	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1084	948	316	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1081	948	316	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1649;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	830	552	184	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	830	552	184	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=946;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1536;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	684	552	184	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	830	552	184	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=637;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=674;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000576024.1	Transcript	synonymous_variant	8	9	3	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1582;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1198	831	277	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1081	831	277	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	830	471	157	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	830	471	157	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	830	471	157	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1084	831	277	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1138	831	277	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1081	831	277	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1091	831	277	P	ccC/ccT	rs1427959882,COSV52880112	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
750727	17:7673580-7673580	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1427959882,COSV52880112	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1085	943	315	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	943	943	315	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs762620193,COSV52761602	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1076	943	315	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1079	943	315	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1076	943	315	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs762620193,COSV52761602	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1644;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	825	547	183	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	825	547	183	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs762620193,COSV52761602	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=941;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs762620193,COSV52761602	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1531;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	679	547	183	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	825	547	183	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs762620193,COSV52761602	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=632;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs762620193,COSV52761602	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=669;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000576024.1	Transcript	missense_variant	3	4	2	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs762620193,COSV52761602	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1577;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1193	826	276	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1076	826	276	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	825	466	156	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	825	466	156	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	825	466	156	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1079	826	276	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1133	826	276	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1076	826	276	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1086	826	276	S/T	Tct/Act	rs762620193,COSV52761602	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
185212	17:7673585-7673585	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs762620193,COSV52761602	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1084	942	314	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	942	942	314	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1075	942	314	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1078	942	314	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1075	942	314	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1643;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	824	546	182	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	824	546	182	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=940;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1530;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	678	546	182	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	824	546	182	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=668;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000576024.1	Transcript	coding_sequence_variant	2	3	1	X	ncC/ncA	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1576;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1192	825	275	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1075	825	275	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	824	465	155	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	824	465	155	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	824	465	155	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1078	825	275	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1132	825	275	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1075	825	275	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1085	825	275	S	tcC/tcA	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458577	17:7673586-7673586	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1084	942	314	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	942	942	314	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1075	942	314	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1078	942	314	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1075	942	314	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1643;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	824	546	182	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	824	546	182	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=940;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1530;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	678	546	182	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	824	546	182	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=668;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000576024.1	Transcript	coding_sequence_variant	2	3	1	X	ncC/ncG	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/2;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1576;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1192	825	275	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1075	825	275	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	824	465	155	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	824	465	155	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	824	465	155	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1078	825	275	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1132	825	275	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1075	825	275	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1085	825	275	S	tcC/tcG	rs765930028,COSV99433274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
745588	17:7673586-7673586	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs765930028,COSV99433274	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1078	936	312	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	936	936	312	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1069	936	312	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1072	936	312	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1069	936	312	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1637;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	818	540	180	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	818	540	180	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=934;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1524;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	672	540	180	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	818	540	180	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=625;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=662;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=5;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1570;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1186	819	273	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1069	819	273	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	818	459	153	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	818	459	153	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	818	459	153	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1072	819	273	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1126	819	273	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1069	819	273	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1079	819	273	T	acC/acA	CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1650075	17:7673592-7673592	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,1,1;PHENO=1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1078	936	312	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	936	936	312	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1069	936	312	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1072	936	312	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1069	936	312	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1637;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	818	540	180	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	818	540	180	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=934;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1524;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	672	540	180	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	818	540	180	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=625;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=662;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=5;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1570;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1186	819	273	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1069	819	273	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	818	459	153	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	818	459	153	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	818	459	153	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1072	819	273	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1126	819	273	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1069	819	273	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1079	819	273	T	acC/acG	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
458576	17:7673592-7673592	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555524991,CD165594,COSV52772076,COSV53210453	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1077	935	312	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	935	935	312	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1068	935	312	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1071	935	312	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1068	935	312	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1636;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	817	539	180	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	817	539	180	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=933;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1523;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	671	539	180	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	817	539	180	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=624;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=661;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=6;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1569;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1185	818	273	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1068	818	273	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	817	458	153	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	817	458	153	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	817	458	153	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1071	818	273	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1125	818	273	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1068	818	273	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1078	818	273	T/N	aCc/aAc	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1766672	17:7673593-7673593	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	CM1613761,COSV52782880,COSV53026048,COSV53067624	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,1,1,1;PHENO=1,1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1075	933	311	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	933	933	311	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs201601993,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1066	933	311	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1069	933	311	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1066	933	311	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs201601993,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1634;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	815	537	179	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	815	537	179	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201601993,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=931;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201601993,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1521;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	669	537	179	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	815	537	179	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201601993,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=622;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs201601993,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=659;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs201601993,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=8;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs201601993,COSV53154719,COSV53486992	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1567;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1183	816	272	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1066	816	272	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	815	456	152	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	815	456	152	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	815	456	152	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1069	816	272	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1123	816	272	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1066	816	272	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1076	816	272	N	aaC/aaT	rs201601993,COSV53154719,COSV53486992	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
387119	17:7673595-7673595	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs201601993,COSV53154719,COSV53486992	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1072	930	310	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	930	930	310	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1063	930	310	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1066	930	310	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1063	930	310	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1631;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	812	534	178	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	812	534	178	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=928;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1518;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	666	534	178	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	812	534	178	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=619;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=656;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=11;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1564;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1180	813	271	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1063	813	271	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	812	453	151	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	812	453	151	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	812	453	151	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1066	813	271	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1120	813	271	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1063	813	271	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1073	813	271	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1766523	17:7673598-7673598	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1072	930	310	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	930	930	310	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs876660829	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1063	930	310	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1066	930	310	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1063	930	310	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660829	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1631;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	812	534	178	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	812	534	178	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660829	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=928;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660829	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1518;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	666	534	178	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	812	534	178	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660829	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=619;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660829	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=656;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660829	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=11;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660829	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1564;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1180	813	271	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1063	813	271	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	812	453	151	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	812	453	151	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	812	453	151	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1066	813	271	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1120	813	271	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1063	813	271	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1073	813	271	N/K	aaC/aaG	rs876660829	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;PHENO=1
428879	17:7673598-7673598	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs876660829	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1071	929	310	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	929	929	310	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52772317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1062	929	310	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1065	929	310	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1062	929	310	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52772317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1630;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	811	533	178	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	811	533	178	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52772317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=927;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52772317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1517;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	665	533	178	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	811	533	178	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52772317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=618;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52772317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52772317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=12;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52772317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1563;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1179	812	271	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1062	812	271	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	811	452	151	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	811	452	151	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	811	452	151	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1065	812	271	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1119	812	271	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1062	812	271	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1072	812	271	N/S	aAc/aGc	COSV52772317	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1766454	17:7673599-7673599	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52772317	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1;PHENO=1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1069	927	309	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	927	927	309	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1060	927	309	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1063	927	309	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1060	927	309	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1628;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	809	531	177	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	809	531	177	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=925;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1515;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	663	531	177	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	809	531	177	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=616;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=653;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1561;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1177	810	270	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1060	810	270	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	809	450	150	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	809	450	150	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	809	450	150	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1063	810	270	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1117	810	270	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1060	810	270	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1070	810	270	P	ccC/ccT	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534893	17:7673601-7673601	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1069	927	309	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	927	927	309	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1060	927	309	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1063	927	309	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1060	927	309	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1628;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	809	531	177	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	809	531	177	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=925;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1515;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	663	531	177	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	809	531	177	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=616;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=653;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1561;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1177	810	270	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1060	810	270	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	809	450	150	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	809	450	150	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	809	450	150	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1063	810	270	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1117	810	270	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1060	810	270	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1070	810	270	P	ccC/ccA	rs1393711933,COSV53371983	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
487001	17:7673601-7673601	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1393711933,COSV53371983	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1066	924	308	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	924	924	308	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1057	924	308	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1060	924	308	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1057	924	308	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1625;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	806	528	176	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	806	528	176	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=922;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1512;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	660	528	176	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	806	528	176	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=613;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=650;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=17;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1558;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1174	807	269	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1057	807	269	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	806	447	149	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	806	447	149	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	806	447	149	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1060	807	269	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1114	807	269	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1057	807	269	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1067	807	269	L	ctG/ctA	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185901	17:7673604-7673604	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs786202546,COSV52782637,COSV53135431,COSV53781699	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	1064	922	308	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,synonymous_variant	922	922	308	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525016,COSV52729154,COSV53317260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,synonymous_variant	1055	922	308	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	1058	922	308	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,synonymous_variant	1055	922	308	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525016,COSV52729154,COSV53317260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1623;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,synonymous_variant	804	526	176	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,synonymous_variant	804	526	176	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525016,COSV52729154,COSV53317260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=920;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525016,COSV52729154,COSV53317260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1510;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,synonymous_variant	658	526	176	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,synonymous_variant	804	526	176	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525016,COSV52729154,COSV53317260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=611;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525016,COSV52729154,COSV53317260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525016,COSV52729154,COSV53317260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=19;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525016,COSV52729154,COSV53317260	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1556;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,synonymous_variant	1172	805	269	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,synonymous_variant	1055	805	269	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,synonymous_variant	804	445	149	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,synonymous_variant	804	445	149	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,synonymous_variant	804	445	149	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,synonymous_variant	1058	805	269	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,synonymous_variant	1112	805	269	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,synonymous_variant	1055	805	269	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,synonymous_variant,NMD_transcript_variant	1065	805	269	L	Ctg/Ttg	rs1555525016,COSV52729154,COSV53317260	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485024	17:7673606-7673606	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525016,COSV52729154,COSV53317260	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	1063	921	307	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,synonymous_variant	921	921	307	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52949946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,synonymous_variant	1054	921	307	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	1057	921	307	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,synonymous_variant	1054	921	307	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52949946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1622;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,synonymous_variant	803	525	175	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,synonymous_variant	803	525	175	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52949946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=919;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52949946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1509;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,synonymous_variant	657	525	175	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,synonymous_variant	803	525	175	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52949946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=610;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52949946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=647;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52949946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=20;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52949946	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1555;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,synonymous_variant	1171	804	268	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,synonymous_variant	1054	804	268	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,synonymous_variant	803	444	148	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,synonymous_variant	803	444	148	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,synonymous_variant	803	444	148	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,synonymous_variant	1057	804	268	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,synonymous_variant	1111	804	268	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,synonymous_variant	1054	804	268	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,synonymous_variant,NMD_transcript_variant	1064	804	268	A	gcA/gcG	COSV52949946	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=9/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1641134	17:7673607-7673607	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52949946	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525022	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525022	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1617;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525022	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=914;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525022	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1504;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525022	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=605;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525022	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=642;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525022	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=25;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525022	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1550;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525022	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
823092	17:7673612-7673612	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525022	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1613;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=910;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1500;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=601;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=638;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=29;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525024	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1546;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525024	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528281	17:7673616-7673616	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525024	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597359848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1611;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=908;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1498;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=599;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=636;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597359848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=31;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597359848	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1544;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1597359848	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793717	17:7673618-7673618	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597359848	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057523270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1610;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=907;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1497;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=598;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=635;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=32;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1543;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1057523270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
388913	17:7673619-7673619	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057523270	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1608;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1495;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=596;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=34;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1541;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1603884	17:7673621-7673621	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1608;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1495;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=596;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=34;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1541;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614433	17:7673621-7673621	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1608;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1495;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=596;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=34;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1541;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1057522354	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385882	17:7673621-7673621	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057522354	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs752627700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs752627700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1607;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752627700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752627700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1494;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752627700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=595;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs752627700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=632;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs752627700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=35;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752627700	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1540;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs752627700	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379596	17:7673622-7673622	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs752627700	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs911934766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs911934766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1604;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs911934766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=901;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs911934766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1491;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs911934766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=592;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs911934766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=629;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs911934766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=38;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs911934766	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1537;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs911934766	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
492626	17:7673625-7673625	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs911934766	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign,benign/likely_benign;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1547;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=844;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1434;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=535;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=572;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=93;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1480;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
420997	17:7673679-7673682	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1064794839	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;PHENO=1
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1548;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=845;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1435;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=536;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=573;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=94;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1481;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1659758	17:7673681-7673681	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1545;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=842;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1432;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=533;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=570;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=97;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1478;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378747	17:7673684-7673684	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057520386	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1543;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=840;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1430;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=531;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=568;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=99;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1476;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389753	17:7673686-7673686	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057523528,COSV53210422	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1541;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=838;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1428;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=529;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=101;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1474;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
517670	17:7673687-7673688	-	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs936119541	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1541;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=838;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1428;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=529;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=566;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=101;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1474;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1536618	17:7673688-7673688	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1537;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=834;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1424;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=525;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=562;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=105;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1470;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378746	17:7673692-7673692	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs772829199	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1536;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=833;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1423;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=524;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=561;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=106;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525043	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1469;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525043	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
528280	17:7673693-7673693	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525043	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs199527475	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs199527475	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1535;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs199527475	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs199527475	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1422;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs199527475	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=523;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs199527475	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=560;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs199527475	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=107;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs199527475	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1468;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs199527475	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387437	17:7673694-7673694	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs199527475	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1058	916	306	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	916	916	306	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1049	916	306	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1052	916	306	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1049	916	306	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1525;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	798	520	174	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	798	520	174	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=822;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1412;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	652	520	174	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	798	520	174	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=513;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=550;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=117;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1458;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1166	799	267	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1049	799	267	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	798	439	147	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	798	439	147	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	798	439	147	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1052	799	267	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1106	799	267	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1049	799	267	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1059	799	267	R	Cga/Aga	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528276	17:7673704-7673704	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs121913344,CM971506,COSV52662281,COSV52987117,COSV53852813	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1057	915	305	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	915	915	305	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52702028,COSV53068075,COSV53188252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1048	915	305	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1051	915	305	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1048	915	305	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52702028,COSV53068075,COSV53188252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1524;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	797	519	173	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	797	519	173	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52702028,COSV53068075,COSV53188252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=821;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52702028,COSV53068075,COSV53188252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1411;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	651	519	173	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	797	519	173	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52702028,COSV53068075,COSV53188252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=512;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52702028,COSV53068075,COSV53188252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52702028,COSV53068075,COSV53188252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=118;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52702028,COSV53068075,COSV53188252	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1457;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1165	798	266	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1048	798	266	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	797	438	146	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	797	438	146	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	797	438	146	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1051	798	266	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1105	798	266	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1048	798	266	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1058	798	266	K	aaG/aaA	COSV52702028,COSV53068075,COSV53188252	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1563452	17:7673705-7673705	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52702028,COSV53068075,COSV53188252	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1,1;PHENO=1,1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1054	912	304	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	912	912	304	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525052,COSV52701088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1045	912	304	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1048	912	304	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1045	912	304	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525052,COSV52701088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1521;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	794	516	172	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	794	516	172	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525052,COSV52701088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=818;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525052,COSV52701088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1408;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	648	516	172	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	794	516	172	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525052,COSV52701088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=509;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525052,COSV52701088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525052,COSV52701088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=121;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525052,COSV52701088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1454;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1162	795	265	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1045	795	265	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	794	435	145	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	794	435	145	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	794	435	145	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1048	795	265	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1102	795	265	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1045	795	265	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1055	795	265	T	acT/acC	rs1555525052,COSV52701088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482208	17:7673708-7673708	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525052,COSV52701088	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1049	907	303	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	907	907	303	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587782391,COSV52729387,COSV53200423	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1040	907	303	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1043	907	303	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1040	907	303	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782391,COSV52729387,COSV53200423	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1516;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	789	511	171	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	789	511	171	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782391,COSV52729387,COSV53200423	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=813;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782391,COSV52729387,COSV53200423	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1403;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	643	511	171	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	789	511	171	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782391,COSV52729387,COSV53200423	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=504;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782391,COSV52729387,COSV53200423	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=541;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782391,COSV52729387,COSV53200423	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=126;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587782391,COSV52729387,COSV53200423	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1449;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1157	790	264	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1040	790	264	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	789	430	144	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	789	430	144	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	789	430	144	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1043	790	264	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1097	790	264	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1040	790	264	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1050	790	264	S/G	Agc/Ggc	rs587782391,COSV52729387,COSV53200423	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
142332	17:7673713-7673713	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs587782391,COSV52729387,COSV53200423	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance,likely_benign,conflicting_interpretations_of_pathogenicity;SOMATIC=0,1,1;PHENO=1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1045	903	301	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	903	903	301	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1036	903	301	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1039	903	301	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1036	903	301	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1512;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	785	507	169	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	785	507	169	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=809;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1399;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	639	507	169	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	785	507	169	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=500;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=537;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=130;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1445;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1153	786	262	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1036	786	262	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	785	426	142	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	785	426	142	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	785	426	142	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1039	786	262	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1093	786	262	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1036	786	262	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1046	786	262	P	ccA/ccG	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184179	17:7673717-7673717	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs72661120,CM121213,COSV52916616,COSV53163330	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=benign,benign/likely_benign,likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1042	900	300	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	900	900	300	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1033	900	300	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1036	900	300	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1033	900	300	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1509;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	782	504	168	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	782	504	168	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=806;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1396;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	636	504	168	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	782	504	168	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=497;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=534;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=133;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1442;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1150	783	261	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1033	783	261	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	782	423	141	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	782	423	141	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	782	423	141	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1036	783	261	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1090	783	261	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1033	783	261	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1043	783	261	P	ccC/ccG	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384686	17:7673720-7673720	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1042	900	300	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	900	900	300	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1033	900	300	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1036	900	300	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1033	900	300	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1509;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	782	504	168	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	782	504	168	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=806;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1396;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	636	504	168	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	782	504	168	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=497;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=534;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=133;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1442;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1150	783	261	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1033	783	261	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	782	423	141	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	782	423	141	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	782	423	141	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1036	783	261	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1090	783	261	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1033	783	261	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1043	783	261	P	ccC/ccT	rs767356182,COSV53486330	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
794149	17:7673720-7673720	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs767356182,COSV53486330	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1041	899	300	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	899	899	300	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs909643864,COSV52712660,COSV53743131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1032	899	300	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1035	899	300	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1032	899	300	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs909643864,COSV52712660,COSV53743131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1508;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	781	503	168	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	781	503	168	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs909643864,COSV52712660,COSV53743131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=805;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs909643864,COSV52712660,COSV53743131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1395;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	635	503	168	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	781	503	168	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs909643864,COSV52712660,COSV53743131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=496;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs909643864,COSV52712660,COSV53743131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=533;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs909643864,COSV52712660,COSV53743131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=134;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs909643864,COSV52712660,COSV53743131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1441;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1149	782	261	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1032	782	261	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	781	422	141	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	781	422	141	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	781	422	141	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1035	782	261	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1089	782	261	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1032	782	261	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1042	782	261	P/L	cCc/cTc	rs909643864,COSV52712660,COSV53743131	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1765377	17:7673721-7673721	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs909643864,COSV52712660,COSV53743131	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,1,1;PHENO=0,1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1039	897	299	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	897	897	299	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1030	897	299	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1033	897	299	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1030	897	299	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1506;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	779	501	167	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	779	501	167	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=803;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1393;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	633	501	167	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	779	501	167	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=531;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=136;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1439;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1147	780	260	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1030	780	260	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	779	420	140	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	779	420	140	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	779	420	140	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1033	780	260	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1087	780	260	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1030	780	260	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1040	780	260	L	ctG/ctA	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765314	17:7673723-7673723	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1039	897	299	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	897	897	299	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1030	897	299	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1033	897	299	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1030	897	299	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1506;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	779	501	167	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	779	501	167	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=803;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1393;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	633	501	167	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	779	501	167	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=494;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=531;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=136;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1439;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1147	780	260	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1030	780	260	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	779	420	140	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	779	420	140	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	779	420	140	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1033	780	260	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1087	780	260	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1030	780	260	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1040	780	260	L	ctG/ctT	COSV52839794,COSV53307293	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1765317	17:7673723-7673723	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52839794,COSV53307293	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1;PHENO=1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1037	895	299	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	895	895	299	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs752701561,COSV53087037,COSV53695760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1028	895	299	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1031	895	299	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1028	895	299	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs752701561,COSV53087037,COSV53695760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1504;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	777	499	167	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	777	499	167	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752701561,COSV53087037,COSV53695760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=801;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752701561,COSV53087037,COSV53695760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1391;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	631	499	167	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	777	499	167	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752701561,COSV53087037,COSV53695760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=492;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs752701561,COSV53087037,COSV53695760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=529;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs752701561,COSV53087037,COSV53695760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=138;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs752701561,COSV53087037,COSV53695760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1437;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1145	778	260	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1028	778	260	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	777	418	140	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	777	418	140	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	777	418	140	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1031	778	260	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1085	778	260	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1028	778	260	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1038	778	260	L	Ctg/Ttg	rs752701561,COSV53087037,COSV53695760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414039	17:7673725-7673725	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs752701561,COSV53087037,COSV53695760	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1036	894	298	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	894	894	298	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1027	894	298	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1030	894	298	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1027	894	298	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1503;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	776	498	166	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	776	498	166	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=800;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1390;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	630	498	166	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	776	498	166	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=491;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=139;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1436;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1144	777	259	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1027	777	259	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	776	417	139	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	776	417	139	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	776	417	139	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1030	777	259	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1084	777	259	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1027	777	259	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1037	777	259	E	gaG/gaA	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528275	17:7673726-7673726	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs756123992,COSV53542087,COSV53684282,COSV53707547	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1033	891	297	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	891	891	297	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs750578863	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1024	891	297	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1027	891	297	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1024	891	297	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs750578863	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1500;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	773	495	165	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	773	495	165	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs750578863	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=797;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs750578863	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1387;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	627	495	165	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	773	495	165	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs750578863	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=488;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs750578863	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=525;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs750578863	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=142;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs750578863	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1433;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1141	774	258	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1024	774	258	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	773	414	138	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	773	414	138	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	773	414	138	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1027	774	258	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1081	774	258	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1024	774	258	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1034	774	258	H	caC/caT	rs750578863	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183849	17:7673729-7673729	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs750578863	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;PHENO=1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1030	888	296	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	888	888	296	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs758395031,COSV52747097,COSV53551410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1021	888	296	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1024	888	296	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1021	888	296	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs758395031,COSV52747097,COSV53551410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1497;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	770	492	164	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	770	492	164	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758395031,COSV52747097,COSV53551410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=794;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758395031,COSV52747097,COSV53551410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1384;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	624	492	164	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	770	492	164	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758395031,COSV52747097,COSV53551410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=485;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs758395031,COSV52747097,COSV53551410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs758395031,COSV52747097,COSV53551410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=145;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs758395031,COSV52747097,COSV53551410	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1430;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1138	771	257	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1021	771	257	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	770	411	137	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	770	411	137	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	770	411	137	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1024	771	257	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1078	771	257	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1021	771	257	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1031	771	257	H	caC/caT	rs758395031,COSV52747097,COSV53551410	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=0,1,1
1764984	17:7673732-7673732	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs758395031,COSV52747097,COSV53551410	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,1,1;PHENO=0,1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1027	885	295	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	885	885	295	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs200073907,COSV52851077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1018	885	295	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1021	885	295	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1018	885	295	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs200073907,COSV52851077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1494;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	767	489	163	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	767	489	163	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200073907,COSV52851077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=791;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200073907,COSV52851077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1381;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	621	489	163	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	767	489	163	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200073907,COSV52851077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=482;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs200073907,COSV52851077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=519;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs200073907,COSV52851077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=148;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200073907,COSV52851077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1427;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1135	768	256	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1018	768	256	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	767	408	136	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	767	408	136	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	767	408	136	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1021	768	256	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1075	768	256	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1018	768	256	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1028	768	256	P	ccT/ccC	rs200073907,COSV52851077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
132754	17:7673735-7673735	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs200073907,COSV52851077	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1024	882	294	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	882	882	294	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52661825,COSV52937308	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1015	882	294	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1018	882	294	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1015	882	294	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661825,COSV52937308	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1491;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	764	486	162	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	764	486	162	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661825,COSV52937308	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=788;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661825,COSV52937308	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1378;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	618	486	162	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	764	486	162	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661825,COSV52937308	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=479;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661825,COSV52937308	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=516;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52661825,COSV52937308	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=151;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661825,COSV52937308	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1424;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1132	765	255	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1015	765	255	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	764	405	135	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	764	405	135	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	764	405	135	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1018	765	255	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1072	765	255	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1015	765	255	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1025	765	255	E	gaG/gaA	COSV52661825,COSV52937308	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140223	17:7673738-7673738	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52661825,COSV52937308	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1;PHENO=1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1021	879	293	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	879	879	293	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1366652292,COSV52751109,COSV52761595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1012	879	293	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1015	879	293	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1012	879	293	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1366652292,COSV52751109,COSV52761595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1488;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	761	483	161	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	761	483	161	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1366652292,COSV52751109,COSV52761595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=785;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1366652292,COSV52751109,COSV52761595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1375;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	615	483	161	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	761	483	161	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1366652292,COSV52751109,COSV52761595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=476;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1366652292,COSV52751109,COSV52761595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=513;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1366652292,COSV52751109,COSV52761595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=154;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1366652292,COSV52751109,COSV52761595	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1421;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1129	762	254	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1012	762	254	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	761	402	134	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	761	402	134	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	761	402	134	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1015	762	254	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1069	762	254	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1012	762	254	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1022	762	254	G	ggG/ggA	rs1366652292,COSV52751109,COSV52761595	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
822744	17:7673741-7673741	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1366652292,COSV52751109,COSV52761595	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1018	876	292	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	876	876	292	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1009	876	292	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1012	876	292	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1009	876	292	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1485;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	758	480	160	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	758	480	160	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=782;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1372;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	612	480	160	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	758	480	160	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=473;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=157;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1418;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1126	759	253	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1009	759	253	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	758	399	133	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	758	399	133	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	758	399	133	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1012	759	253	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1066	759	253	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1009	759	253	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1019	759	253	K	aaA/aaG	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
923496	17:7673744-7673744	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2073180917,COSV52795860,COSV53037721,COSV53188887	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1017	875	292	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	875	875	292	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	1008	875	292	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1011	875	292	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	1008	875	292	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1484;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	757	479	160	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	757	479	160	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=781;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1371;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	611	479	160	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	757	479	160	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=472;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=509;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=158;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1417;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1125	758	253	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	1008	758	253	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	757	398	133	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	757	398	133	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	757	398	133	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1011	758	253	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1065	758	253	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	1008	758	253	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1018	758	253	K/R	aAa/aGa	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
406577	17:7673745-7673745	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs121912663,CM994791,COSV53008143,COSV53067424,COSV99066499	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1012	870	290	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	870	870	290	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1003	870	290	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1006	870	290	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1003	870	290	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1479;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	752	474	158	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	752	474	158	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=776;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1366;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	606	474	158	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	752	474	158	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=467;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=504;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=163;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1412;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1120	753	251	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1003	753	251	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	752	393	131	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	752	393	131	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	752	393	131	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1006	753	251	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1060	753	251	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1003	753	251	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1013	753	251	R	cgC/cgA	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
514422	17:7673750-7673750	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525135,COSV52918863,COSV53622711,COSV53637296,COSV53741507	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1009	867	289	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	867	867	289	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1000	867	289	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1003	867	289	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1000	867	289	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1476;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	749	471	157	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	749	471	157	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=773;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1363;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	603	471	157	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	749	471	157	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=464;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=166;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1409;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1117	750	250	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1000	750	250	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	749	390	130	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	749	390	130	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	749	390	130	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1003	750	250	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1057	750	250	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1000	750	250	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1010	750	250	L	ctC/ctT	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233110	17:7673753-7673753	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1009	867	289	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	867	867	289	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	1000	867	289	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	1003	867	289	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	1000	867	289	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1476;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	749	471	157	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	749	471	157	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=773;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1363;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	603	471	157	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	749	471	157	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=464;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=501;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=166;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1409;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1117	750	250	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	1000	750	250	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	749	390	130	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	749	390	130	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	749	390	130	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	1003	750	250	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1057	750	250	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	1000	750	250	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1010	750	250	L	ctC/ctG	rs778138282,COSV52736208,COSV53026071	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
764207	17:7673753-7673753	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs778138282,COSV52736208,COSV53026071	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	1008	866	289	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	866	866	289	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	999	866	289	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	1002	866	289	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	999	866	289	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1475;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	748	470	157	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	748	470	157	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=772;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1362;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	602	470	157	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	748	470	157	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=463;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=500;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=167;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1408;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1116	749	250	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	999	749	250	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	748	389	130	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	748	389	130	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	748	389	130	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	1002	749	250	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	1056	749	250	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	999	749	250	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	1009	749	250	L/P	cTc/cCc	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1172923	17:7673754-7673754	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52783014,COSV52988671,COSV53770961	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1,1;PHENO=1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	1003	861	287	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	861	861	287	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	994	861	287	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	997	861	287	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	994	861	287	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1470;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	743	465	155	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	743	465	155	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=767;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1357;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	597	465	155	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	743	465	155	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=458;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=495;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=172;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1403;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1111	744	248	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	994	744	248	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	743	384	128	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	743	384	128	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	743	384	128	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	997	744	248	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1051	744	248	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	994	744	248	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	1004	744	248	E	gaG/gaA	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1764064	17:7673759-7673759	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52684280,COSV52840253,COSV52883064,COSV99362734	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1,1,1;PHENO=1,1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	997	855	285	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	855	855	285	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1487868349,COSV52933457,COSV52950642	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	988	855	285	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	991	855	285	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	988	855	285	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1487868349,COSV52933457,COSV52950642	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1464;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	737	459	153	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	737	459	153	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1487868349,COSV52933457,COSV52950642	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=761;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1487868349,COSV52933457,COSV52950642	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1351;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	591	459	153	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	737	459	153	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1487868349,COSV52933457,COSV52950642	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=452;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1487868349,COSV52933457,COSV52950642	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=489;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1487868349,COSV52933457,COSV52950642	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=178;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1487868349,COSV52933457,COSV52950642	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1397;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1105	738	246	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	988	738	246	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	737	378	126	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	737	378	126	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	737	378	126	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	991	738	246	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1045	738	246	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	988	738	246	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	998	738	246	E	gaG/gaA	rs1487868349,COSV52933457,COSV52950642	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492625	17:7673765-7673765	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1487868349,COSV52933457,COSV52950642	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	994	852	284	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	852	852	284	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	985	852	284	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	988	852	284	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	985	852	284	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1461;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	734	456	152	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	734	456	152	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=758;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1348;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	588	456	152	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	734	456	152	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=449;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=486;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=181;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1394;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1102	735	245	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	985	735	245	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	734	375	125	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	734	375	125	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	734	375	125	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	988	735	245	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1042	735	245	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	985	735	245	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	995	735	245	T	acA/acC	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186509	17:7673768-7673768	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	994	852	284	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	852	852	284	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	985	852	284	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	988	852	284	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	985	852	284	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1461;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	734	456	152	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	734	456	152	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=758;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1348;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	588	456	152	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	734	456	152	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=449;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=486;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=181;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1394;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1102	735	245	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	985	735	245	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	734	375	125	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	734	375	125	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	734	375	125	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	988	735	245	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1042	735	245	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	985	735	245	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	995	735	245	T	acA/acG	rs786203004,COSV53098088	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
798589	17:7673768-7673768	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs786203004,COSV53098088	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	991	849	283	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	849	849	283	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	982	849	283	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	985	849	283	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	982	849	283	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1458;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	731	453	151	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	731	453	151	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=755;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1345;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	585	453	151	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	731	453	151	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=446;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=483;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=184;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1391;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1099	732	244	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	982	732	244	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	731	372	124	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	731	372	124	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	731	372	124	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	985	732	244	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1039	732	244	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	982	732	244	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	992	732	244	R	cgC/cgG	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
458570	17:7673771-7673771	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525197,COSV52772770,COSV52907973,COSV53232948,COSV53577753	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	988	846	282	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	846	846	282	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525211,COSV53037261,COSV53156241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	979	846	282	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	982	846	282	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	979	846	282	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525211,COSV53037261,COSV53156241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1455;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	728	450	150	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	728	450	150	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525211,COSV53037261,COSV53156241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=752;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525211,COSV53037261,COSV53156241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1342;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	582	450	150	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	728	450	150	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525211,COSV53037261,COSV53156241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=443;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525211,COSV53037261,COSV53156241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=480;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525211,COSV53037261,COSV53156241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=187;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525211,COSV53037261,COSV53156241	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1388;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1096	729	243	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	979	729	243	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	728	369	123	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	728	369	123	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	728	369	123	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	982	729	243	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1036	729	243	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	979	729	243	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	989	729	243	R	cgG/cgA	rs1555525211,COSV53037261,COSV53156241	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492624	17:7673774-7673774	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555525211,COSV53037261,COSV53156241	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	986	844	282	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	844	844	282	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	977	844	282	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	980	844	282	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	977	844	282	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1453;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	726	448	150	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	726	448	150	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=750;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1340;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	580	448	150	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	726	448	150	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=441;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=478;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=189;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1386;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1094	727	243	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	977	727	243	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	726	367	123	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	726	367	123	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	726	367	123	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	980	727	243	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1034	727	243	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	977	727	243	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	987	727	243	R	Cgg/Agg	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1531579	17:7673776-7673776	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	CM056413,CM920678,COSV52662048,COSV52662222,COSV52701296	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	985	843	281	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	843	843	281	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	976	843	281	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	979	843	281	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	976	843	281	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1452;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	725	447	149	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	725	447	149	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=749;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1339;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	579	447	149	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	725	447	149	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=440;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=477;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=190;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1385;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1093	726	242	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	976	726	242	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	725	366	122	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	725	366	122	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	725	366	122	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	979	726	242	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1033	726	242	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	976	726	242	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	986	726	242	D	gaC/gaT	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
669380	17:7673777-7673777	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057519984,CM137620,COSV52664212,COSV52688790,COSV52719382,COSV53103731	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	980	838	280	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	838	838	280	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	971	838	280	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	974	838	280	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	971	838	280	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1447;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	720	442	148	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	720	442	148	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=744;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1334;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	574	442	148	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	720	442	148	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=435;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=472;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=195;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1380;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1088	721	241	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	971	721	241	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	720	361	121	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	720	361	121	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	720	361	121	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	974	721	241	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1028	721	241	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	971	721	241	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	981	721	241	R	Aga/Cga	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
926213	17:7673782-7673782	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs753660142,COSV52662754,COSV52708728,COSV52851287	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	979	837	279	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	837	837	279	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	970	837	279	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	973	837	279	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	970	837	279	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	719	441	147	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	719	441	147	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=743;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1333;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	573	441	147	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	719	441	147	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=434;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=471;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=196;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1379;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1087	720	240	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	970	720	240	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	719	360	120	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	719	360	120	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	719	360	120	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	973	720	240	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1027	720	240	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	970	720	240	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	980	720	240	G	ggG/ggA	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
184190	17:7673783-7673783	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs786201322,CD963012,COSV53098982,COSV53696473	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1;PHENO=1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	973	831	277	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	831	831	277	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	964	831	277	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	967	831	277	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	964	831	277	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1440;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	713	435	145	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	713	435	145	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=737;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1327;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	567	435	145	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	713	435	145	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=428;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=465;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=202;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1373;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1081	714	238	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	964	714	238	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	713	354	118	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	713	354	118	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	713	354	118	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	967	714	238	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1021	714	238	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	964	714	238	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	974	714	238	C	tgT/tgC	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
389164	17:7673789-7673789	G	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057523347,CM065496,COSV52676368,COSV52783531,COSV53164903	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	970	828	276	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	828	828	276	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	961	828	276	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	964	828	276	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	961	828	276	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1437;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	710	432	144	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	710	432	144	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=734;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1324;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	564	432	144	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	710	432	144	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=425;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=462;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=205;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1370;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1078	711	237	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	961	711	237	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	710	351	117	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	710	351	117	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	710	351	117	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	964	711	237	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1018	711	237	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	961	711	237	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	971	711	237	A	gcC/gcT	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1084600	17:7673792-7673792	A	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	970	828	276	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	828	828	276	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	961	828	276	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	964	828	276	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	961	828	276	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1437;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	710	432	144	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	710	432	144	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=734;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1324;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	564	432	144	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	710	432	144	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=425;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=462;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=205;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1370;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1078	711	237	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	961	711	237	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	710	351	117	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	710	351	117	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	710	351	117	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	964	711	237	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1018	711	237	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	961	711	237	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	971	711	237	A	gcC/gcA	COSV52796700,COSV52814873,COSV52939371	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1762752	17:7673792-7673792	T	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52796700,COSV52814873,COSV52939371	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1,1;PHENO=1,1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	964	822	274	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	822	822	274	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52751885,COSV53327229	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	955	822	274	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	958	822	274	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	955	822	274	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52751885,COSV53327229	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1431;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	704	426	142	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	704	426	142	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52751885,COSV53327229	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=728;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52751885,COSV53327229	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1318;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	558	426	142	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	704	426	142	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52751885,COSV53327229	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=419;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52751885,COSV53327229	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=456;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52751885,COSV53327229	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=211;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52751885,COSV53327229	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1364;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1072	705	235	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	955	705	235	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	704	345	115	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	704	345	115	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	704	345	115	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	958	705	235	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1012	705	235	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	955	705	235	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	965	705	235	V	gtT/gtG	COSV52751885,COSV53327229	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1161148	17:7673798-7673798	C	-	ENSR00000548580	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52751885,COSV53327229	IMPACT=MODIFIER;BIOTYPE=CTCF_binding_site;SOMATIC=1,1;PHENO=1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	958	816	272	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	816	816	272	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	949	816	272	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	952	816	272	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	949	816	272	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1425;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	698	420	140	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	698	420	140	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=722;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1312;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	552	420	140	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	698	420	140	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=413;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=450;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=217;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1358;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1066	699	233	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	949	699	233	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	698	339	113	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	698	339	113	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	698	339	113	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	952	699	233	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1006	699	233	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	949	699	233	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1136213	17:7673804-7673804	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	959	699	233	V	gtG/gtA	rs756421198,COSV52918960,COSV53313340,COSV53438396	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	955	813	271	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	813	813	271	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	946	813	271	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	949	813	271	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	946	813	271	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1422;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	695	417	139	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	695	417	139	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=719;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1309;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	549	417	139	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	695	417	139	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=410;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=447;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=220;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1355;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1063	696	232	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	946	696	232	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	695	336	112	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	695	336	112	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	695	336	112	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	949	696	232	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	1003	696	232	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	946	696	232	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1635919	17:7673807-7673807	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	956	696	232	E	gaG/gaA	rs1567548081,COSV52661621,COSV52849794,COSV52892313,COSV53037823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	946	804	268	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	804	804	268	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597362168,COSV53086682,COSV53241270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	937	804	268	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	940	804	268	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	937	804	268	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362168,COSV53086682,COSV53241270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1413;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	686	408	136	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	686	408	136	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362168,COSV53086682,COSV53241270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=710;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362168,COSV53086682,COSV53241270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1300;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	540	408	136	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	686	408	136	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362168,COSV53086682,COSV53241270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=401;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362168,COSV53086682,COSV53241270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=438;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597362168,COSV53086682,COSV53241270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=229;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362168,COSV53086682,COSV53241270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1346;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1054	687	229	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	937	687	229	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	686	327	109	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	686	327	109	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	686	327	109	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	940	687	229	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	994	687	229	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	937	687	229	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827414	17:7673816-7673816	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	947	687	229	N	aaC/aaT	rs1597362168,COSV53086682,COSV53241270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	943	801	267	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	801	801	267	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	934	801	267	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	937	801	267	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	934	801	267	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1410;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	683	405	135	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	683	405	135	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=707;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1297;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	537	405	135	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	683	405	135	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=398;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=435;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=232;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1343;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1051	684	228	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	934	684	228	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	683	324	108	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	683	324	108	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	683	324	108	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	937	684	228	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	991	684	228	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	934	684	228	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1761696	17:7673819-7673819	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	944	684	228	R	cgG/cgT	COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	943	801	267	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	801	801	267	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	934	801	267	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	937	801	267	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	934	801	267	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1410;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	683	405	135	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	683	405	135	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=707;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1297;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	537	405	135	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	683	405	135	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=398;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=435;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=232;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1343;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1051	684	228	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	934	684	228	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	683	324	108	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	683	324	108	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	683	324	108	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	937	684	228	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	991	684	228	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	934	684	228	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827400	17:7673819-7673819	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	944	684	228	R	cgG/cgA	rs1597362195,COSV52712702,COSV53164528,COSV53387047	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	940	798	266	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	798	798	266	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	931	798	266	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	934	798	266	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	931	798	266	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1407;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	680	402	134	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	680	402	134	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=704;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1294;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	534	402	134	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	680	402	134	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=395;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=432;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=235;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1340;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1048	681	227	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	931	681	227	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	680	321	107	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	680	321	107	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	680	321	107	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	934	681	227	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	988	681	227	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	931	681	227	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
487002	17:7673822-7673822	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	941	681	227	G	ggA/ggT	rs1555525321,COSV52700790,COSV53141063,COSV53424760	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	937	795	265	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	795	795	265	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	928	795	265	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	931	795	265	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	928	795	265	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1404;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	677	399	133	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	677	399	133	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=701;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1291;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	531	399	133	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	677	399	133	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=392;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=429;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=238;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1337;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1045	678	226	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	928	678	226	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	677	318	106	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	677	318	106	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	677	318	106	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	931	678	226	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	985	678	226	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	928	678	226	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827359	17:7673825-7673825	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	938	678	226	L	ctG/ctT	rs1285844180,COSV52661636,COSV52730242,COSV52895662,COSV99474023	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	934	792	264	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	792	792	264	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	925	792	264	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	928	792	264	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	925	792	264	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1401;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	674	396	132	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	674	396	132	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=698;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1288;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	528	396	132	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	674	396	132	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=389;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=426;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=241;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1334;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1042	675	225	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	925	675	225	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	674	315	105	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	674	315	105	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	674	315	105	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	928	675	225	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	982	675	225	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	925	675	225	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1761262	17:7673828-7673828	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	935	675	225	L	ctA/ctT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	934	792	264	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	792	792	264	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1060504162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	925	792	264	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	928	792	264	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	925	792	264	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060504162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1401;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	674	396	132	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	674	396	132	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060504162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=698;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060504162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1288;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	528	396	132	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	674	396	132	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060504162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=389;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060504162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=426;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=241;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060504162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1334;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1042	675	225	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	925	675	225	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	674	315	105	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	674	315	105	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	674	315	105	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	928	675	225	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	982	675	225	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	925	675	225	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414027	17:7673828-7673828	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	935	675	225	L	ctA/ctG	rs1060504162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	931	789	263	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	789	789	263	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs770598448,COSV52935703,COSV53210322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	922	789	263	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	925	789	263	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	922	789	263	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs770598448,COSV52935703,COSV53210322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1398;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	671	393	131	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	671	393	131	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs770598448,COSV52935703,COSV53210322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=695;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs770598448,COSV52935703,COSV53210322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1285;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	525	393	131	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	671	393	131	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs770598448,COSV52935703,COSV53210322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=386;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs770598448,COSV52935703,COSV53210322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=423;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs770598448,COSV52935703,COSV53210322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=244;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs770598448,COSV52935703,COSV53210322	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1331;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1039	672	224	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	922	672	224	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	671	312	104	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	671	312	104	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	671	312	104	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	925	672	224	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	979	672	224	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	922	672	224	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
549727	17:7673831-7673831	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	932	672	224	N	aaT/aaC	rs770598448,COSV52935703,COSV53210322	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	930	788	263	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	788	788	263	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597362411,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	921	788	263	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	924	788	263	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	921	788	263	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362411,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1397;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	670	392	131	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	670	392	131	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362411,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=694;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362411,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1284;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	524	392	131	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	670	392	131	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362411,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=385;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362411,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=422;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597362411,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=245;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597362411,COSV53208998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1330;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1038	671	224	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	921	671	224	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	670	311	104	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	670	311	104	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	670	311	104	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	924	671	224	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	978	671	224	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	921	671	224	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
827313	17:7673832-7673832	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	931	671	224	N/S	aAt/aGt	rs1597362411,COSV53208998	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=8/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1386;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=683;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1273;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=374;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=411;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=256;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1319;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1160239	17:7673843-7673843	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	COSV105031836,COSV105875862,COSV53743733	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs771914358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs771914358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1381;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs771914358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=678;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs771914358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1268;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs771914358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=369;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs771914358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=406;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs771914358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=261;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs771914358	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1314;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492613	17:7673848-7673848	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs771914358	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1380;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=677;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1267;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=368;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=405;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=262;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1313;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1554415	17:7673849-7673849	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1379;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=676;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1266;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=367;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=404;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=263;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525373	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1312;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548875	17:7673850-7673850	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525373	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1379;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=676;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1266;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=367;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=404;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=263;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1312;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919077	17:7673850-7673850	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1378;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=675;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1265;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=366;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=403;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=264;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1311;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919427	17:7673851-7673851	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs774987850,COSV53596362	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1359;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=656;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1246;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=347;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=384;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=283;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1292;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492614	17:7673870-7673870	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs113302588	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1358;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1245;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=346;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=383;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=284;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1291;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627658	17:7673871-7673871	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs376988747	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1357;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=654;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1244;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=345;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=382;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=285;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1290;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492615	17:7673872-7673872	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs776659879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1346;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=643;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1233;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=334;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=371;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=296;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1279;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
924456	17:7673883-7673883	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2073214106	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1345;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=642;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1232;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=333;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=370;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=297;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1278;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628282	17:7673884-7673884	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1337240615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1340;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=637;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1227;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=328;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=365;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=302;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1273;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492616	17:7673889-7673889	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs774455868	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1336;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1223;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=324;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=361;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=306;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1269;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630945	17:7673893-7673893	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567548516	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1334;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1221;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=322;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=359;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=308;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1267;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492617	17:7673895-7673895	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1334;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=631;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1221;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=322;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=359;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=308;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1267;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
627846	17:7673895-7673895	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1343035495	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1333;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1220;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=321;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=358;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=309;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1266;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492618	17:7673896-7673896	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs774077441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1332;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=629;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1219;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=320;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=357;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=310;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1265;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492619	17:7673897-7673897	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs898427453	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1330;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1217;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=318;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=355;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=312;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1263;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492620	17:7673899-7673899	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1328;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=625;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1215;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=316;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=353;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=314;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1261;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629937	17:7673901-7673901	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs995865613	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1326;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=623;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1213;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=314;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=351;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=316;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1259;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492621	17:7673903-7673903	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525382	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1314;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=611;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1201;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=302;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=339;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=328;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1247;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492622	17:7673914-7673915	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525386	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1311;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=608;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1198;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=299;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=336;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=331;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1244;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922786	17:7673918-7673918	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2073217850	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1140;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=437;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1027;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=128;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=165;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=502;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1073;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243959	17:7674089-7674089	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs12951053,COSV52747988	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1120;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=417;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1007;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=108;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=145;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1053;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1243351	17:7674109-7674109	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs12947788,COSV52747994	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1066;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=363;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=953;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=54;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=91;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=576;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=999;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1616913	17:7674163-7674163	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	COSV52761579	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1065;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=362;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=952;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=53;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=90;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=577;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=998;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
137692	17:7674164-7674164	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs17880172,COSV53407727,COSV53533660	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1062;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=359;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=949;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=50;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=87;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=580;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=995;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492612	17:7674167-7674167	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1437756379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1058;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=355;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=945;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=46;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=83;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=584;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=991;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
378745	17:7674171-7674171	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs200277687,COSV52677858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1056;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=353;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=943;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=44;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=81;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=586;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=989;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1121811	17:7674173-7674173	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597363720	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1056;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597363720	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=353;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597363720	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=943;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597363720	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=44;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597363720	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=81;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597363720	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=586;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597363720	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=989;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
754552	17:7674173-7674173	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1597363720	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622076	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1054;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622076	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=351;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622076	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=941;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622076	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=42;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622076	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=79;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs864622076	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs864622076	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=987;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
219416	17:7674174-7674175	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs864622076	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1051;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=348;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=938;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=39;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=76;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=591;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=984;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_donor_region_variant,intron_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
565601	17:7674178-7674178	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_donor_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525425,COSV52863867	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	911	769	257	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	769	769	257	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	769	769	257	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	902	769	257	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	905	769	257	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	902	769	257	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs779761818,COSV52717368,COSV53120630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1035;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	651	373	125	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	651	373	125	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs779761818,COSV52717368,COSV53120630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=332;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs779761818,COSV52717368,COSV53120630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=922;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	505	373	125	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	651	373	125	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs779761818,COSV52717368,COSV53120630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=23;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs779761818,COSV52717368,COSV53120630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=60;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs779761818,COSV52717368,COSV53120630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=607;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs779761818,COSV52717368,COSV53120630	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=968;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1019	652	218	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	902	652	218	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	651	292	98	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	651	292	98	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	651	292	98	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	905	652	218	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	959	652	218	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	902	652	218	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233767	17:7674194-7674194	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	912	652	218	L	Ctg/Ttg	rs779761818,COSV52717368,COSV53120630	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	910	768	256	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	768	768	256	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	768	768	256	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	901	768	256	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	904	768	256	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	901	768	256	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1034;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	650	372	124	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	650	372	124	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=331;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=921;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	504	372	124	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	650	372	124	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=22;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=59;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=608;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=967;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1018	651	217	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	901	651	217	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	650	291	97	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	650	291	97	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	650	291	97	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	904	651	217	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	958	651	217	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	901	651	217	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1760134	17:7674195-7674195	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	911	651	217	T	acA/acC	COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	910	768	256	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	768	768	256	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	768	768	256	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	901	768	256	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	904	768	256	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	901	768	256	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1034;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	650	372	124	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	650	372	124	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=331;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=921;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	504	372	124	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	650	372	124	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=22;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=59;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=608;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=967;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1018	651	217	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	901	651	217	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	650	291	97	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	650	291	97	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	650	291	97	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	904	651	217	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	958	651	217	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	901	651	217	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187222	17:7674195-7674195	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	911	651	217	T	acA/acG	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	910	768	256	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	768	768	256	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	768	768	256	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	901	768	256	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	904	768	256	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	901	768	256	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1034;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	650	372	124	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	650	372	124	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=331;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=921;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	504	372	124	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	650	372	124	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=22;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=59;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=608;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203563,COSV52838755	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=967;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1018	651	217	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	901	651	217	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	650	291	97	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	650	291	97	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	650	291	97	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	904	651	217	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	958	651	217	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	901	651	217	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492611	17:7674195-7674195	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	911	651	217	T	acA/acT	rs786203563,COSV52838755	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	907	765	255	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	765	765	255	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	765	765	255	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	898	765	255	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	901	765	255	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	898	765	255	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53124648,COSV53233921,COSV53651156	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1031;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	647	369	123	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	647	369	123	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53124648,COSV53233921,COSV53651156	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=328;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53124648,COSV53233921,COSV53651156	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=918;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	501	369	123	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	647	369	123	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53124648,COSV53233921,COSV53651156	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=19;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53124648,COSV53233921,COSV53651156	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=56;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53124648,COSV53233921,COSV53651156	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=611;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53124648,COSV53233921,COSV53651156	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=964;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1015	648	216	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	898	648	216	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	647	288	96	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	647	288	96	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	647	288	96	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	901	648	216	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	955	648	216	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	898	648	216	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1532094	17:7674198-7674198	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	908	648	216	I	atC/atT	COSV53124648,COSV53233921,COSV53651156	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	904	762	254	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	762	762	254	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	762	762	254	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	895	762	254	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	898	762	254	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	895	762	254	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52849548,COSV53510655,COSV53833684	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1028;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	644	366	122	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	644	366	122	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52849548,COSV53510655,COSV53833684	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=325;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52849548,COSV53510655,COSV53833684	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=915;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	498	366	122	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	644	366	122	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52849548,COSV53510655,COSV53833684	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=16;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52849548,COSV53510655,COSV53833684	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=53;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52849548,COSV53510655,COSV53833684	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=614;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52849548,COSV53510655,COSV53833684	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=961;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1012	645	215	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	895	645	215	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	644	285	95	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	644	285	95	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	644	285	95	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	898	645	215	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	952	645	215	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	895	645	215	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
923830	17:7674201-7674201	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	905	645	215	I	atC/atT	COSV52849548,COSV53510655,COSV53833684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	902	760	254	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	760	760	254	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	760	760	254	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	893	760	254	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	896	760	254	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	893	760	254	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1026;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	642	364	122	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	642	364	122	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=323;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=913;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	496	364	122	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	642	364	122	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=51;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=616;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=959;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1010	643	215	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	893	643	215	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	642	283	95	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	642	283	95	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	642	283	95	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	896	643	215	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	950	643	215	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	893	643	215	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
406605	17:7674203-7674203	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	903	643	215	I/V	Atc/Gtc	rs746601313,COSV52784505,COSV52825280,COSV52872554,COSV52987059	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	898	756	252	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	756	756	252	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	756	756	252	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	889	756	252	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	892	756	252	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	889	756	252	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1022;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	638	360	120	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	638	360	120	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=319;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=909;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	492	360	120	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	638	360	120	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=10;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=47;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=955;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1006	639	213	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	889	639	213	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	638	279	93	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	638	279	93	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	638	279	93	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	892	639	213	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	946	639	213	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	889	639	213	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759568	17:7674207-7674207	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	899	639	213	L	ctC/ctT	COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	898	756	252	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	756	756	252	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	756	756	252	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	889	756	252	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	892	756	252	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	889	756	252	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1022;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	638	360	120	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	638	360	120	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=319;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=909;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	492	360	120	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	638	360	120	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=10;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=47;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=955;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1006	639	213	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	889	639	213	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	638	279	93	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	638	279	93	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	638	279	93	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	892	639	213	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	946	639	213	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	889	639	213	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
827129	17:7674207-7674207	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	899	639	213	L	ctC/ctA	rs1597364197,COSV52937189,COSV53099988,COSV53120416,COSV53368158	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	896	754	252	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	754	754	252	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	754	754	252	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	887	754	252	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	890	754	252	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	887	754	252	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1020;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	636	358	120	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	636	358	120	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=317;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=907;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	490	358	120	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	636	358	120	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=8;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=45;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=622;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52730003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=953;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	1004	637	213	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	887	637	213	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	636	277	93	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	636	277	93	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	636	277	93	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	890	637	213	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	944	637	213	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	887	637	213	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1759470	17:7674209-7674209	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	897	637	213	L/V	Ctc/Gtc	COSV52730003	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	895	753	251	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	753	753	251	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	753	753	251	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	886	753	251	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	889	753	251	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	886	753	251	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1019;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	635	357	119	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	635	357	119	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=316;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=906;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	489	357	119	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	635	357	119	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=7;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=44;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=623;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=952;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	1003	636	212	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	886	636	212	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	635	276	92	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	635	276	92	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	635	276	92	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	889	636	212	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	943	636	212	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	886	636	212	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
237955	17:7674210-7674210	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	896	636	212	I	atC/atT	rs878854074,CM951231,COSV52689050,COSV52978618,COSV53202810	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	889	747	249	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	747	747	249	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	747	747	249	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	880	747	249	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	883	747	249	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	880	747	249	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661594,COSV52668882,COSV52827572	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1013;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	629	351	117	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	629	351	117	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661594,COSV52668882,COSV52827572	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=310;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661594,COSV52668882,COSV52827572	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=900;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	483	351	117	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	629	351	117	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000514944.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661594,COSV52668882,COSV52827572	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661594,COSV52668882,COSV52827572	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=38;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52661594,COSV52668882,COSV52827572	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=629;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661594,COSV52668882,COSV52827572	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=946;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	997	630	210	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	880	630	210	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	629	270	90	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	629	270	90	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	629	270	90	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	883	630	210	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	937	630	210	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	880	630	210	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1555468	17:7674216-7674216	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	890	630	210	R	agG/agA	COSV52661594,COSV52668882,COSV52827572	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	887	745	249	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	745	745	249	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	745	745	249	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	878	745	249	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	881	745	249	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	878	745	249	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1011;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	627	349	117	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	627	349	117	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=308;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=898;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	481	349	117	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	627	349	117	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000514944.5	Transcript	incomplete_terminal_codon_variant,coding_sequence_variant	545	466	156	X	Ag/Cg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=36;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=631;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=944;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	995	628	210	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	878	628	210	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	627	268	90	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	627	268	90	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	627	268	90	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	881	628	210	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	935	628	210	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	878	628	210	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1759002	17:7674218-7674218	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	888	628	210	R	Agg/Cgg	COSV52662247,COSV52676356,COSV52892337,COSV52908430	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	886	744	248	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	744	744	248	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	744	744	248	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	877	744	248	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	880	744	248	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	877	744	248	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52782654,COSV53050697,COSV53372256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1010;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	626	348	116	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	626	348	116	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52782654,COSV53050697,COSV53372256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=307;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52782654,COSV53050697,COSV53372256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=897;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	480	348	116	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	626	348	116	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	544	465	155	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52782654,COSV53050697,COSV53372256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=35;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52782654,COSV53050697,COSV53372256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=632;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52782654,COSV53050697,COSV53372256	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=943;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	994	627	209	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	877	627	209	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	626	267	89	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	626	267	89	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	626	267	89	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	880	627	209	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	934	627	209	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	877	627	209	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1758970	17:7674219-7674219	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	887	627	209	R	cgG/cgA	COSV52782654,COSV53050697,COSV53372256	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	884	742	248	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	742	742	248	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	742	742	248	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	875	742	248	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	878	742	248	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	875	742	248	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1008;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	624	346	116	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	624	346	116	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=305;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	478	346	116	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	624	346	116	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	542	463	155	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=33;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=634;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=941;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	992	625	209	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	875	625	209	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	624	265	89	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	624	265	89	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	624	265	89	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	878	625	209	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	932	625	209	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	875	625	209	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
918353	17:7674221-7674221	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	885	625	209	R	Cgg/Agg	CM010465,CM900211,COSV52662035,COSV52797251,COSV53097881	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	883	741	247	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	741	741	247	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	741	741	247	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	874	741	247	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	877	741	247	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	874	741	247	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1007;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	623	345	115	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	623	345	115	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=304;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=894;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	477	345	115	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	623	345	115	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	541	462	154	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=32;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=635;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=940;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	991	624	208	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	874	624	208	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	623	264	88	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	623	264	88	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	623	264	88	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	877	624	208	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	931	624	208	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	874	624	208	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185778	17:7674222-7674222	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	884	624	208	N	aaC/aaT	rs786202448,COSV52772996,COSV52808615,COSV52847658	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	874	732	244	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	732	732	244	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	732	732	244	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	865	732	244	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	868	732	244	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	865	732	244	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=998;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	614	336	112	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	614	336	112	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=295;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=885;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	468	336	112	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	614	336	112	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	532	453	151	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=23;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=644;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=931;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	982	615	205	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	865	615	205	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	614	255	85	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	614	255	85	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	614	255	85	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	868	615	205	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	922	615	205	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	865	615	205	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1099444	17:7674231-7674231	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	875	615	205	G	ggC/ggA	COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	874	732	244	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	732	732	244	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	732	732	244	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	865	732	244	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	868	732	244	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	865	732	244	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=998;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	614	336	112	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	614	336	112	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=295;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=885;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	468	336	112	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	614	336	112	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	532	453	151	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=23;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=644;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=931;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	982	615	205	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	865	615	205	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	614	255	85	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	614	255	85	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	614	255	85	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	868	615	205	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	922	615	205	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	865	615	205	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
219796	17:7674231-7674231	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	875	615	205	G	ggC/ggT	rs759625762,COSV52677306,COSV52755988,COSV52773862,COSV53128429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	865	723	241	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	723	723	241	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	723	723	241	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	856	723	241	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	859	723	241	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	856	723	241	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53025058,COSV53153033,COSV53211006	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=989;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	605	327	109	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	605	327	109	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53025058,COSV53153033,COSV53211006	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=286;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53025058,COSV53153033,COSV53211006	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=876;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	459	327	109	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	605	327	109	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	523	444	148	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53025058,COSV53153033,COSV53211006	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=14;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53025058,COSV53153033,COSV53211006	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=653;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53025058,COSV53153033,COSV53211006	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=922;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	973	606	202	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	856	606	202	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	605	246	82	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	605	246	82	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	605	246	82	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	859	606	202	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	913	606	202	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	856	606	202	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1757851	17:7674240-7674240	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	866	606	202	S	tcC/tcT	COSV53025058,COSV53153033,COSV53211006	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	859	717	239	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	717	717	239	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	717	717	239	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	850	717	239	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	853	717	239	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	850	717	239	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=983;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	599	321	107	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	599	321	107	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=280;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=870;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	453	321	107	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	599	321	107	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	517	438	146	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000574684.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=659;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=916;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	967	600	200	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	850	600	200	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	599	240	80	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	599	240	80	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	599	240	80	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	853	600	200	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	907	600	200	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	850	600	200	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480762	17:7674246-7674246	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	860	600	200	N	aaC/aaT	rs1057522275,COSV52752124,COSV52877093,COSV52983691	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	850	708	236	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	708	708	236	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	708	708	236	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	841	708	236	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	844	708	236	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	841	708	236	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=974;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	590	312	104	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	590	312	104	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=271;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=861;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	444	312	104	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	590	312	104	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	508	429	143	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	103	-	-	-	-	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=668;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=907;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	958	591	197	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	841	591	197	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	590	231	77	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	590	231	77	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	590	231	77	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	844	591	197	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	898	591	197	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	841	591	197	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
796361	17:7674255-7674255	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	851	591	197	Y	taC/taT	rs1597365202,CD951866,COSV52713084,COSV52728511,COSV53025106,COSV53864205	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	847	705	235	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	705	705	235	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	705	705	235	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	838	705	235	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	841	705	235	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	838	705	235	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs750893877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	587	309	103	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	587	309	103	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs750893877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=268;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs750893877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	441	309	103	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	587	309	103	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	505	426	142	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	100	-	-	-	-	rs750893877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs750893877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=671;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs750893877	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	955	588	196	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	838	588	196	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	587	228	76	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	587	228	76	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	587	228	76	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	841	588	196	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	895	588	196	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	838	588	196	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1096768	17:7674258-7674258	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	848	588	196	N	aaC/aaT	rs750893877	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	841	699	233	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	699	699	233	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	699	699	233	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	832	699	233	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	835	699	233	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	832	699	233	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52850817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=965;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	581	303	101	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	581	303	101	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52850817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=262;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52850817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=852;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	435	303	101	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	581	303	101	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	499	420	140	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	94	-	-	-	-	COSV52850817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52850817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=677;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52850817	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=898;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	949	582	194	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	832	582	194	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	581	222	74	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	581	222	74	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	581	222	74	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	835	582	194	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	889	582	194	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	832	582	194	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1099079	17:7674264-7674264	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	842	582	194	H	caC/caT	COSV52850817	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	838	696	232	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	696	696	232	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	696	696	232	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	829	696	232	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	832	696	232	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	829	696	232	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=962;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	578	300	100	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	578	300	100	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=259;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=849;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	432	300	100	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	578	300	100	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	496	417	139	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	91	-	-	-	-	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=680;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	946	579	193	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	829	579	193	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	578	219	73	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	578	219	73	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	578	219	73	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	832	579	193	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	886	579	193	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	829	579	193	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
186360	17:7674267-7674267	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	839	579	193	I	atC/atT	rs786202888,COSV105030456,COSV53101286,COSV53649861	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	835	693	231	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	693	693	231	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	693	693	231	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	826	693	231	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	829	693	231	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	826	693	231	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52775800,COSV52880748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=959;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	575	297	99	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	575	297	99	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52775800,COSV52880748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=256;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52775800,COSV52880748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=846;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	429	297	99	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	575	297	99	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	493	414	138	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	88	-	-	-	-	COSV52775800,COSV52880748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52775800,COSV52880748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52775800,COSV52880748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	943	576	192	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	826	576	192	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	575	216	72	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	575	216	72	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	575	216	72	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	829	576	192	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	883	576	192	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	826	576	192	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1672974	17:7674270-7674270	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	836	576	192	T	acC/acT	COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	835	693	231	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	693	693	231	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	693	693	231	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	826	693	231	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	829	693	231	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	826	693	231	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073265072,COSV52775800,COSV52880748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=959;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	575	297	99	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	575	297	99	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073265072,COSV52775800,COSV52880748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=256;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073265072,COSV52775800,COSV52880748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=846;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	429	297	99	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	575	297	99	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	493	414	138	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	88	-	-	-	-	rs2073265072,COSV52775800,COSV52880748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073265072,COSV52775800,COSV52880748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs2073265072,COSV52775800,COSV52880748	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	943	576	192	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	826	576	192	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	575	216	72	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	575	216	72	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	575	216	72	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	829	576	192	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	883	576	192	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	826	576	192	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
919788	17:7674270-7674270	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	836	576	192	T	acC/acA	rs2073265072,COSV52775800,COSV52880748	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	829	687	229	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	687	687	229	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	687	687	229	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	820	687	229	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	823	687	229	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	820	687	229	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CD076915,COSV52903842,COSV53757768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=953;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	569	291	97	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	569	291	97	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD076915,COSV52903842,COSV53757768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=250;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD076915,COSV52903842,COSV53757768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=840;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	423	291	97	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	569	291	97	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	487	408	136	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	82	-	-	-	-	CD076915,COSV52903842,COSV53757768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD076915,COSV52903842,COSV53757768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=689;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD076915,COSV52903842,COSV53757768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=886;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	937	570	190	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	820	570	190	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	569	210	70	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	569	210	70	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	569	210	70	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	823	570	190	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	877	570	190	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	820	570	190	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
1315753	17:7674276-7674276	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	830	570	190	C	tgT/tgC	CD076915,COSV52903842,COSV53757768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1;PHENO=1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	823	681	227	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	681	681	227	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	681	681	227	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	814	681	227	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	817	681	227	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	814	681	227	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=947;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	563	285	95	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	563	285	95	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=244;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=834;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	417	285	95	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	563	285	95	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	481	402	134	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	76	-	-	-	-	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=695;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=880;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	931	564	188	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	814	564	188	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	563	204	68	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	563	204	68	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	563	204	68	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	817	564	188	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	871	564	188	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	814	564	188	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
481159	17:7674282-7674282	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	824	564	188	S	tcT/tcG	rs1555525574,COSV52809847,COSV53096994,COSV53684875,COSV53828814	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	820	678	226	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	678	678	226	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	678	678	226	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	811	678	226	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	814	678	226	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	811	678	226	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs916168683,COSV52688852,COSV52994759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=944;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	560	282	94	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	560	282	94	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs916168683,COSV52688852,COSV52994759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=241;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs916168683,COSV52688852,COSV52994759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=831;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	414	282	94	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	560	282	94	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	478	399	133	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	73	-	-	-	-	rs916168683,COSV52688852,COSV52994759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs916168683,COSV52688852,COSV52994759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=698;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs916168683,COSV52688852,COSV52994759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=877;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	928	561	187	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	811	561	187	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	560	201	67	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	560	201	67	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	560	201	67	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	814	561	187	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	868	561	187	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	811	561	187	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
506707	17:7674285-7674285	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	821	561	187	G	ggC/ggA	rs916168683,COSV52688852,COSV52994759	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	817	675	225	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,synonymous_variant	675	675	225	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,synonymous_variant	675	675	225	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,synonymous_variant	808	675	225	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	811	675	225	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,synonymous_variant	808	675	225	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525584,COSV52891821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=941;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,synonymous_variant	557	279	93	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,synonymous_variant	557	279	93	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525584,COSV52891821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=238;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525584,COSV52891821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=828;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,synonymous_variant	411	279	93	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,synonymous_variant	557	279	93	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,synonymous_variant	475	396	132	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000574684.1	Transcript	splice_region_variant,non_coding_transcript_exon_variant	70	-	-	-	-	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=2/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525584,COSV52891821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=701;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525584,COSV52891821	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=874;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,synonymous_variant	925	558	186	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,synonymous_variant	808	558	186	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,synonymous_variant	557	198	66	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,synonymous_variant	557	198	66	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,synonymous_variant	557	198	66	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,synonymous_variant	811	558	186	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,synonymous_variant	865	558	186	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,synonymous_variant	808	558	186	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485025	17:7674288-7674288	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,synonymous_variant,NMD_transcript_variant	818	558	186	V	gtT/gtC	rs1555525584,COSV52891821	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=7/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658684	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=934;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658684	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=231;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658684	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=821;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000574684.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658684	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=708;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876658684	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=867;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
230648	17:7674295-7674295	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs876658684	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=930;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=227;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=817;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000574684.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=712;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=863;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
406576	17:7674298-7674299	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs762540407,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=930;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=227;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=817;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000574684.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=712;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=863;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
629931	17:7674299-7674299	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs754628512,COSV53134509	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=927;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=224;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=814;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000574684.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=715;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=860;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1531221	17:7674302-7674302	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=926;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=223;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=813;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000574684.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=716;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525587	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492586	17:7674303-7674303	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525587	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs780893609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=924;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs780893609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=221;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs780893609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=811;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000574684.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs780893609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs780893609	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=857;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1621986	17:7674305-7674305	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs780893609	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=921;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=218;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=808;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=721;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=854;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1673177	17:7674308-7674308	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	COSV53283525	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=920;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=217;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=807;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=722;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=853;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
379595	17:7674309-7674309	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs564974117,COSV52766964	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=903;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=200;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=790;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=739;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=836;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
221184	17:7674326-7674326	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs17880604,CS004882,COSV52683791	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=902;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=199;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=789;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=740;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=835;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
371964	17:7674327-7674327	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs374907737	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=192;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=782;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=747;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=828;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1755156	17:7674334-7674334	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1261337213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=839;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=136;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=726;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=803;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=772;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1187478	17:7674390-7674390	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs183276131	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=703;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000505014.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=0;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=590;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=938;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=636;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677776	17:7674525-7674525	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs539331761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=590;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	1148	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=477;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1052;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=523;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
677733	17:7674639-7674639	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs8069054,COSV104369758	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=432;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	990	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=319;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1210;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=365;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
256603	17:7674797-7674797	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1625895	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=418;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	976	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=305;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1224;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=351;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1194751	17:7674811-7674811	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=418;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	976	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=305;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1224;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=351;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1326387	17:7674811-7674811	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs17884607	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=405;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	963	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=292;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1237;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=338;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133419	17:7674824-7674824	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs587778001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=not_provided;PHENO=1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=401;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	959	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=288;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1241;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=334;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
133420	17:7674828-7674828	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs34949160,COSV52745548	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1467799984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=378;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	936-950	-	-	-	-	rs1467799984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1467799984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=265;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1467799984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1467799984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1250;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1467799984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=311;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458554	17:7674836-7674851	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1467799984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=389;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	947	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=276;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1253;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=322;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492585	17:7674840-7674840	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1385638165	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=388;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	946	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=275;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1254;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=321;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
182947	17:7674841-7674841	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs199578278,COSV53479395	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=385;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	943	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=272;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1257;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=318;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
383397	17:7674844-7674844	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=385;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	943	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=272;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1257;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=318;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492583	17:7674844-7674844	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs140756213	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	808	666	222	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	666	666	222	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	666	666	222	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	799	666	222	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	802	666	222	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	799	666	222	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=364;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	548	270	90	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	548	270	90	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	922	-	-	-	-	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=251;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	402	270	90	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	548	270	90	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	466	387	129	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1278;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=297;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	916	549	183	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	799	549	183	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	548	189	63	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	548	189	63	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	548	189	63	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	802	549	183	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	856	549	183	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	799	549	183	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
132972	17:7674865-7674865	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	809	549	183	P	ccG/ccT	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	808	666	222	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	666	666	222	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	666	666	222	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	799	666	222	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	802	666	222	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	799	666	222	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=364;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	548	270	90	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	548	270	90	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	922	-	-	-	-	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=251;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	402	270	90	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	548	270	90	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	466	387	129	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1278;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=297;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	916	549	183	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	799	549	183	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	548	189	63	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	548	189	63	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	548	189	63	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	802	549	183	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	856	549	183	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	799	549	183	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187714	17:7674865-7674865	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	809	549	183	P	ccG/ccA	rs72661118,COSV52826471,COSV53267642,COSV53563768	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	802	660	220	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	660	660	220	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	660	660	220	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	793	660	220	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	796	660	220	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	793	660	220	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=358;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	542	264	88	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	542	264	88	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	916	-	-	-	-	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=245;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	396	264	88	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	542	264	88	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	460	381	127	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1284;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=291;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	910	543	181	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	793	543	181	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	542	183	61	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	542	183	61	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	542	183	61	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	796	543	181	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	850	543	181	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	793	543	181	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754475	17:7674871-7674871	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	803	543	181	Y	taT/taC	CD101595,COSV52775381,COSV52839743,COSV53289049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	799	657	219	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	657	657	219	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	657	657	219	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	790	657	219	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	793	657	219	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	790	657	219	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=355;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	539	261	87	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	539	261	87	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	913	-	-	-	-	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=242;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	393	261	87	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	539	261	87	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	457	378	126	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1287;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=288;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	907	540	180	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	790	540	180	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	539	180	60	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	539	180	60	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	539	180	60	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	793	540	180	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	847	540	180	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	790	540	180	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
185002	17:7674874-7674874	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	800	540	180	P	ccC/ccA	rs786201859,COSV52965002,COSV53107694,COSV53515706	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	796	654	218	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	654	654	218	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	654	654	218	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	787	654	218	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	790	654	218	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	787	654	218	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53387326	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=352;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	536	258	86	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	536	258	86	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	910	-	-	-	-	COSV53387326	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53387326	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=239;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	390	258	86	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	536	258	86	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	454	375	125	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV53387326	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53387326	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1290;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53387326	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=285;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	904	537	179	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	787	537	179	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	536	177	59	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	536	177	59	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	536	177	59	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	790	537	179	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	844	537	179	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	787	537	179	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1754155	17:7674877-7674877	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	797	537	179	V	gtG/gtT	COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	796	654	218	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	654	654	218	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	654	654	218	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	787	654	218	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	790	654	218	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	787	654	218	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs753630563,COSV53387326	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=352;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	536	258	86	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	536	258	86	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	910	-	-	-	-	rs753630563,COSV53387326	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs753630563,COSV53387326	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=239;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	390	258	86	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	536	258	86	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	454	375	125	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs753630563,COSV53387326	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs753630563,COSV53387326	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1290;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs753630563,COSV53387326	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=285;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	904	537	179	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	787	537	179	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	536	177	59	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	536	177	59	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	536	177	59	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	790	537	179	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	844	537	179	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	787	537	179	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186048	17:7674877-7674877	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	797	537	179	V	gtG/gtA	rs753630563,COSV53387326	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	793	651	217	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	651	651	217	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	651	651	217	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	784	651	217	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	787	651	217	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	784	651	217	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52997144,COSV53387338	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=349;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	533	255	85	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	533	255	85	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	907	-	-	-	-	COSV52997144,COSV53387338	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52997144,COSV53387338	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=236;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	387	255	85	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	533	255	85	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	451	372	124	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52997144,COSV53387338	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52997144,COSV53387338	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1293;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52997144,COSV53387338	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=282;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	901	534	178	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	784	534	178	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	533	174	58	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	533	174	58	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	533	174	58	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	787	534	178	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	841	534	178	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	784	534	178	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1100550	17:7674880-7674880	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	794	534	178	V	gtG/gtC	COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	793	651	217	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	651	651	217	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	651	651	217	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	784	651	217	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	787	651	217	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	784	651	217	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525747,COSV52997144,COSV53387338	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=349;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	533	255	85	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	533	255	85	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	907	-	-	-	-	rs1555525747,COSV52997144,COSV53387338	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525747,COSV52997144,COSV53387338	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=236;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	387	255	85	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	533	255	85	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	451	372	124	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525747,COSV52997144,COSV53387338	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525747,COSV52997144,COSV53387338	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1293;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525747,COSV52997144,COSV53387338	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=282;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	901	534	178	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	784	534	178	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	533	174	58	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	533	174	58	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	533	174	58	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	787	534	178	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	841	534	178	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	784	534	178	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492581	17:7674880-7674880	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	794	534	178	V	gtG/gtT	rs1555525747,COSV52997144,COSV53387338	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	790	648	216	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	648	648	216	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	648	648	216	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	781	648	216	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	784	648	216	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	781	648	216	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs199693249,COSV105027021	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=346;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	530	252	84	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	530	252	84	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	904	-	-	-	-	rs199693249,COSV105027021	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs199693249,COSV105027021	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=233;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	384	252	84	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	530	252	84	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	448	369	123	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs199693249,COSV105027021	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs199693249,COSV105027021	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1296;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs199693249,COSV105027021	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=279;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	898	531	177	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	781	531	177	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	530	171	57	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	530	171	57	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	530	171	57	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	784	531	177	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	838	531	177	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	781	531	177	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
481169	17:7674883-7674883	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	791	531	177	V	gtG/gtA	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	790	648	216	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	648	648	216	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	648	648	216	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	781	648	216	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	784	648	216	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	781	648	216	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs199693249,COSV105027021	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=346;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	530	252	84	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	530	252	84	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	904	-	-	-	-	rs199693249,COSV105027021	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs199693249,COSV105027021	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=233;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	384	252	84	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	530	252	84	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	448	369	123	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs199693249,COSV105027021	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs199693249,COSV105027021	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1296;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs199693249,COSV105027021	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=279;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	898	531	177	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	781	531	177	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	530	171	57	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	530	171	57	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	530	171	57	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	784	531	177	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	838	531	177	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	781	531	177	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
826438	17:7674883-7674883	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	791	531	177	V	gtG/gtC	rs199693249,COSV105027021	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	787	645	215	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	645	645	215	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	645	645	215	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	778	645	215	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	781	645	215	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	778	645	215	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=343;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	527	249	83	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	527	249	83	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	901	-	-	-	-	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=230;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	381	249	83	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	527	249	83	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	445	366	122	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1299;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=276;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	895	528	176	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	778	528	176	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	527	168	56	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	527	168	56	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	527	168	56	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	781	528	176	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	835	528	176	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	778	528	176	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
630834	17:7674886-7674886	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	788	528	176	S	agT/agC	rs1057520001,CD941799,COSV52752255,COSV52783847,COSV52798196	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	784	642	214	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	642	642	214	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	642	642	214	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	775	642	214	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	778	642	214	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	775	642	214	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=340;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	524	246	82	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	524	246	82	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	898	-	-	-	-	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=227;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	378	246	82	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	524	246	82	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	442	363	121	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1302;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=273;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	892	525	175	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	775	525	175	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	524	165	55	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	524	165	55	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	524	165	55	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	778	525	175	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	832	525	175	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	775	525	175	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
528279	17:7674889-7674889	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	785	525	175	H	caT/caC	rs587781386,COSV52806263,COSV52926654,COSV53527694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	781	639	213	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	639	639	213	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	639	639	213	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	772	639	213	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	775	639	213	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	772	639	213	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=337;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	521	243	81	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	521	243	81	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	895	-	-	-	-	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=224;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	375	243	81	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	521	243	81	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	439	360	120	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1305;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=270;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	889	522	174	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	772	522	174	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	521	162	54	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	521	162	54	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	521	162	54	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	775	522	174	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	829	522	174	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	772	522	174	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
43591	17:7674892-7674892	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	782	522	174	R	cgA/cgG	rs1800372,CM157005,CX984230,COSV52679610,COSV53646820	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,0,1,1;PHENO=1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	779	637	213	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	637	637	213	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	637	637	213	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	770	637	213	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	773	637	213	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	770	637	213	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=335;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	519	241	81	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	519	241	81	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	893	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=222;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	373	241	81	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	519	241	81	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	437	358	120	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1307;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=268;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	887	520	174	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	770	520	174	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	519	160	54	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	519	160	54	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	519	160	54	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	773	520	174	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	827	520	174	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	770	520	174	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826368	17:7674894-7674894	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	780	520	174	R	Cga/Aga	rs397516436,CM951226,COSV52665560,COSV52740638,COSV52746781,COSV52782151	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	775	633	211	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	633	633	211	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	633	633	211	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	766	633	211	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	769	633	211	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	766	633	211	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=331;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	515	237	79	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	515	237	79	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	889	-	-	-	-	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=218;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	369	237	79	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	515	237	79	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	433	354	118	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1311;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=264;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	883	516	172	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	766	516	172	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	515	156	52	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	515	156	52	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	515	156	52	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	769	516	172	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	823	516	172	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	766	516	172	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
826334	17:7674898-7674898	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	776	516	172	T	acT/acG	rs976434163,COSV52699870,COSV52730558,COSV52978317	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	772	630	210	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	630	630	210	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	630	630	210	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	763	630	210	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	766	630	210	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	763	630	210	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=328;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	512	234	78	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	512	234	78	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	886	-	-	-	-	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=215;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	366	234	78	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	512	234	78	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	430	351	117	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1314;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=261;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	880	513	171	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	763	513	171	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	512	153	51	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	512	153	51	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	512	153	51	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	766	513	171	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	820	513	171	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	763	513	171	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482221	17:7674901-7674901	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	773	513	171	N	aaC/aaT	rs1555525791,COSV52937432,COSV53297001,COSV53588238	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	767	625	209	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	625	625	209	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	625	625	209	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	758	625	209	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	761	625	209	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	758	625	209	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=323;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	507	229	77	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	507	229	77	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	881	-	-	-	-	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=210;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	361	229	77	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	507	229	77	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	425	346	116	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1319;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=256;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	875	508	170	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	758	508	170	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	507	148	50	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	507	148	50	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	507	148	50	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	761	508	170	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	815	508	170	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	758	508	170	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1752471	17:7674906-7674906	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	768	508	170	R	Aga/Cga	CM971504,COSV105032558,COSV52741360,COSV52840233,COSV53599366	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	766	624	208	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	624	624	208	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	624	624	208	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	757	624	208	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	760	624	208	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	757	624	208	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761304,COSV53327097	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=322;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	506	228	76	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	506	228	76	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	880	-	-	-	-	COSV52761304,COSV53327097	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761304,COSV53327097	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=209;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	360	228	76	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	506	228	76	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	424	345	115	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52761304,COSV53327097	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52761304,COSV53327097	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1320;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52761304,COSV53327097	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=255;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	874	507	169	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	757	507	169	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	506	147	49	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	506	147	49	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	506	147	49	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	760	507	169	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	814	507	169	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	757	507	169	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1136749	17:7674907-7674907	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	767	507	169	D	gaC/gaT	COSV52761304,COSV53327097	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	764	622	208	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	622	622	208	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	622	622	208	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	755	622	208	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	758	622	208	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	755	622	208	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=320;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	504	226	76	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	504	226	76	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	878	-	-	-	-	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=207;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	358	226	76	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	504	226	76	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	422	343	115	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1322;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=253;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	872	505	169	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	755	505	169	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	504	145	49	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	504	145	49	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	504	145	49	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	758	505	169	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	812	505	169	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	755	505	169	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1752332	17:7674909-7674909	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	765	505	169	D/N	Gac/Aac	COSV52919029,COSV53016463,COSV53587568	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	760	618	206	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	618	618	206	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	618	618	206	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	751	618	206	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	754	618	206	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	751	618	206	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=316;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	500	222	74	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	500	222	74	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	874	-	-	-	-	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=203;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	354	222	74	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	500	222	74	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	418	339	113	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1326;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=249;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	868	501	167	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	751	501	167	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	500	141	47	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	500	141	47	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	500	141	47	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	754	501	167	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	808	501	167	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	751	501	167	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183903	17:7674913-7674913	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	761	501	167	L	ttG/ttA	rs142813240,COSV53153155,COSV53170603,COSV53438297	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	758	616	206	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	616	616	206	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	616	616	206	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	749	616	206	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	752	616	206	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	749	616	206	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368418,COSV105876406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=314;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	498	220	74	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	498	220	74	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	872	-	-	-	-	rs1597368418,COSV105876406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368418,COSV105876406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=201;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	352	220	74	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	498	220	74	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	416	337	113	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597368418,COSV105876406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597368418,COSV105876406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1328;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597368418,COSV105876406	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=247;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	866	499	167	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	749	499	167	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	498	139	47	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	498	139	47	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	498	139	47	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	752	499	167	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	806	499	167	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	749	499	167	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
759435	17:7674915-7674915	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	759	499	167	L	Ttg/Ctg	rs1597368418,COSV105876406	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	757	615	205	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	615	615	205	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	615	615	205	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	748	615	205	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	751	615	205	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	748	615	205	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=313;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	497	219	73	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	497	219	73	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	871	-	-	-	-	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=200;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	351	219	73	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	497	219	73	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	415	336	112	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1329;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=246;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	865	498	166	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	748	498	166	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	497	138	46	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	497	138	46	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	497	138	46	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	751	498	166	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	805	498	166	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	748	498	166	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
458553	17:7674916-7674916	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	758	498	166	Y	taT/taC	rs786202222,COSV52713698,COSV52808763,COSV52840738	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	754	612	204	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	612	612	204	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	612	612	204	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	745	612	204	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	748	612	204	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	745	612	204	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs749629973,COSV52750941,COSV52878039	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=310;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	494	216	72	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	494	216	72	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	868	-	-	-	-	rs749629973,COSV52750941,COSV52878039	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs749629973,COSV52750941,COSV52878039	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=197;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	348	216	72	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	494	216	72	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	412	333	111	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs749629973,COSV52750941,COSV52878039	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs749629973,COSV52750941,COSV52878039	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1332;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs749629973,COSV52750941,COSV52878039	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=243;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	862	495	165	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	745	495	165	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	494	135	45	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	494	135	45	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	494	135	45	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	748	495	165	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	802	495	165	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	745	495	165	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184873	17:7674919-7674919	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	755	495	165	E	gaG/gaA	rs749629973,COSV52750941,COSV52878039	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	748	606	202	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	606	606	202	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	606	606	202	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	739	606	202	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	742	606	202	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	739	606	202	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1392931620,COSV52773537,COSV53578083	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=304;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	488	210	70	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	488	210	70	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	862	-	-	-	-	rs1392931620,COSV52773537,COSV53578083	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1392931620,COSV52773537,COSV53578083	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=191;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	342	210	70	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	488	210	70	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	406	327	109	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1392931620,COSV52773537,COSV53578083	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1392931620,COSV52773537,COSV53578083	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1338;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1392931620,COSV52773537,COSV53578083	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=237;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	856	489	163	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	739	489	163	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	488	129	43	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	488	129	43	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	488	129	43	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	742	489	163	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	796	489	163	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	739	489	163	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
458552	17:7674925-7674925	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	749	489	163	R	cgT/cgC	rs1392931620,COSV52773537,COSV53578083	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	739	597	199	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	597	597	199	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	597	597	199	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	730	597	199	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	733	597	199	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	730	597	199	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52688073,COSV53235388	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=295;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	479	201	67	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	479	201	67	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	853	-	-	-	-	COSV52688073,COSV53235388	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52688073,COSV53235388	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=182;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	333	201	67	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	479	201	67	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	397	318	106	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52688073,COSV53235388	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52688073,COSV53235388	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1347;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52688073,COSV53235388	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=228;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	847	480	160	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	730	480	160	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	479	120	40	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	479	120	40	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	479	120	40	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	733	480	160	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	787	480	160	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	730	480	160	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1750808	17:7674934-7674934	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	740	480	160	G	ggA/ggC	COSV52688073,COSV53235388	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	727	585	195	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	585	585	195	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	585	585	195	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	718	585	195	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	721	585	195	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	718	585	195	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=283;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	467	189	63	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	467	189	63	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	841	-	-	-	-	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=170;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	321	189	63	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	467	189	63	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	385	306	102	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1359;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=216;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	835	468	156	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	718	468	156	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	467	108	36	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	467	108	36	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	467	108	36	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	721	468	156	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	775	468	156	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	718	468	156	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480768	17:7674946-7674946	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	728	468	156	I	atC/atA	rs1057519994,COSV52966960,COSV53427713,COSV99394424	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	724	582	194	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	582	582	194	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	582	582	194	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	715	582	194	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	718	582	194	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	715	582	194	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=280;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	464	186	62	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	464	186	62	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	838	-	-	-	-	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=167;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	318	186	62	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	464	186	62	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	382	303	101	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1362;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=213;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	832	465	155	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	715	465	155	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	464	105	35	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	464	105	35	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	464	105	35	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	718	465	155	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	772	465	155	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	715	465	155	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
135950	17:7674949-7674949	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	725	465	155	L	ctT/ctC	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	724	582	194	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	582	582	194	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	582	582	194	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	715	582	194	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	718	582	194	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	715	582	194	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=280;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	464	186	62	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	464	186	62	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	838	-	-	-	-	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=167;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	318	186	62	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	464	186	62	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	382	303	101	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1362;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=213;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	832	465	155	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	715	465	155	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	464	105	35	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	464	105	35	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	464	105	35	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	718	465	155	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	772	465	155	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	715	465	155	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825998	17:7674949-7674949	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	725	465	155	L	ctT/ctA	rs370216745,COSV52772013,COSV52864400,COSV53143214	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	718	576	192	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	576	576	192	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	576	576	192	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	709	576	192	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	712	576	192	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	709	576	192	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=274;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	458	180	60	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	458	180	60	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	832	-	-	-	-	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=161;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	312	180	60	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	458	180	60	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	376	297	99	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1368;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=207;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	826	459	153	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	709	459	153	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	458	99	33	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	458	99	33	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	458	99	33	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	712	459	153	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	766	459	153	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	709	459	153	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
988617	17:7674955-7674955	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	719	459	153	Q/H	caG/caC	COSV53020321,COSV53164604,COSV53577379	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	715	573	191	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	573	573	191	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	573	573	191	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	706	573	191	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	709	573	191	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	706	573	191	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53772983,COSV99359984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=271;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	455	177	59	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	455	177	59	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	829	-	-	-	-	COSV53772983,COSV99359984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53772983,COSV99359984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=158;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	309	177	59	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	455	177	59	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	373	294	98	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV53772983,COSV99359984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53772983,COSV99359984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1371;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53772983,COSV99359984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=204;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	823	456	152	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	706	456	152	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	455	96	32	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	455	96	32	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	455	96	32	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	709	456	152	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	763	456	152	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	706	456	152	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1127789	17:7674958-7674958	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	716	456	152	P	ccT/ccG	COSV53772983,COSV99359984	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	712	570	190	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	570	570	190	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	570	570	190	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	703	570	190	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	706	570	190	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	703	570	190	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52772342	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=268;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	452	174	58	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	452	174	58	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	826	-	-	-	-	COSV52772342	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52772342	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=155;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	306	174	58	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	452	174	58	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	370	291	97	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52772342	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52772342	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1374;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52772342	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=201;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	820	453	151	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	703	453	151	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	452	93	31	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	452	93	31	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	452	93	31	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	706	453	151	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	760	453	151	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	703	453	151	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1110621	17:7674961-7674961	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	713	453	151	P	ccT/ccG	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	712	570	190	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	570	570	190	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	570	570	190	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	703	570	190	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	706	570	190	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	703	570	190	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52772342	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=268;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	452	174	58	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	452	174	58	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	826	-	-	-	-	COSV52772342	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52772342	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=155;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	306	174	58	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	452	174	58	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	370	291	97	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV52772342	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52772342	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1374;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52772342	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=201;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	820	453	151	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	703	453	151	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	452	93	31	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	452	93	31	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	452	93	31	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	706	453	151	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	760	453	151	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	703	453	151	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1560310	17:7674961-7674961	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	713	453	151	P	ccT/ccC	COSV52772342	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	709	567	189	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	567	567	189	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	567	567	189	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	700	567	189	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	703	567	189	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	700	567	189	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs55764374,COSV52730721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=265;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	449	171	57	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	449	171	57	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	823	-	-	-	-	rs55764374,COSV52730721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs55764374,COSV52730721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=152;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	303	171	57	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	449	171	57	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	367	288	96	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs55764374,COSV52730721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs55764374,COSV52730721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1377;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs55764374,COSV52730721	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=198;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	817	450	150	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	700	450	150	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	449	90	30	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	449	90	30	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	449	90	30	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	703	450	150	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	757	450	150	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	700	450	150	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482219	17:7674964-7674964	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	710	450	150	A	gcC/gcT	rs55764374,COSV52730721	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	706	564	188	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	564	564	188	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	564	564	188	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	697	564	188	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	700	564	188	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	697	564	188	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057521837,COSV53108812	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=262;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	446	168	56	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	446	168	56	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	820	-	-	-	-	rs1057521837,COSV53108812	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=5/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057521837,COSV53108812	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=149;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	300	168	56	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	446	168	56	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	364	285	95	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1057521837,COSV53108812	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057521837,COSV53108812	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1380;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057521837,COSV53108812	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=195;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	814	447	149	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	697	447	149	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	446	87	29	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	446	87	29	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	446	87	29	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	700	447	149	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	754	447	149	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	697	447	149	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384057	17:7674967-7674967	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	707	447	149	L	ctG/ctA	rs1057521837,COSV53108812	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=6/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=254;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=141;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1388;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=187;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
755152	17:7674975-7674975	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1597369010,COSV52741566	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=252;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=139;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1390;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=185;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
528282	17:7674977-7674977	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525929,COSV53637246	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=247;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=134;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1392;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=180;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1098166	17:7674978-7674982	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=250;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=137;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1391;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525931	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=183;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458550	17:7674978-7674978	CAAT	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525931	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs373797299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=250;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs373797299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=137;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs373797299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs373797299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1392;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs373797299	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=183;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
215474	17:7674979-7674979	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs373797299	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,benign,likely_benign;PHENO=1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=249;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=136;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1393;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=182;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
514755	17:7674979-7674980	-	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525933,CD931244	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53015762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=244;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53015762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=131;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV53015762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53015762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1398;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53015762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=177;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1583473	17:7674985-7674985	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=244;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=131;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1398;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=177;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630873	17:7674985-7674985	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567552335,COSV53015762	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525938	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=243;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525938	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=130;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555525938	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555525938	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1399;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555525938	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=176;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492580	17:7674986-7674986	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555525938	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=240;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=127;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1402;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=173;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1537986	17:7674989-7674989	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1189939264	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=200;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=87;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1442;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=133;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492749	17:7675029-7675029	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs56181208,COSV53470337	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=196;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=83;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=129;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492579	17:7675033-7675033	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs547244762,COSV53203496	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=190;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=77;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1452;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=123;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1593554	17:7675039-7675039	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=189;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=76;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1453;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=122;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
511585	17:7675040-7675040	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs56226808,COSV53684290	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=188;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000504290.5	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000504937.5	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=75;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000510385.5	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000574684.1	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1454;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=121;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000610623.4	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000618944.4	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000619186.4	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1534118	17:7675041-7675041	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	COSV53145487	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1429928926	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=183;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=4/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1429928926	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=70;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000574684.1	Transcript	splice_region_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;INTRON=1/1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1429928926	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1459;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1429928926	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=116;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1546465	17:7675046-7675046	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1429928926	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	700	558	186	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,synonymous_variant	558	558	186	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,synonymous_variant	558	558	186	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,synonymous_variant	691	558	186	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	694	558	186	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,synonymous_variant	691	558	186	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs375275361,COSV52677455,COSV53407442	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=175;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000504290.5	Transcript	splice_region_variant,synonymous_variant	440	162	54	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000504937.5	Transcript	splice_region_variant,synonymous_variant	440	162	54	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	814	-	-	-	-	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375275361,COSV52677455,COSV53407442	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=62;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,synonymous_variant	294	162	54	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000510385.5	Transcript	splice_region_variant,synonymous_variant	440	162	54	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,synonymous_variant	358	279	93	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000574684.1	Transcript	splice_region_variant,non_coding_transcript_exon_variant	66	-	-	-	-	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs375275361,COSV52677455,COSV53407442	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1467;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs375275361,COSV52677455,COSV53407442	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=108;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,synonymous_variant	808	441	147	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,synonymous_variant	691	441	147	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000610623.4	Transcript	splice_region_variant,synonymous_variant	440	81	27	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000618944.4	Transcript	splice_region_variant,synonymous_variant	440	81	27	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000619186.4	Transcript	splice_region_variant,synonymous_variant	440	81	27	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,synonymous_variant	694	441	147	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,synonymous_variant	748	441	147	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,synonymous_variant	691	441	147	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184048	17:7675054-7675054	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,synonymous_variant,NMD_transcript_variant	701	441	147	D	gaT/gaC	rs375275361,COSV52677455,COSV53407442	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	698	556	186	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	556	556	186	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	556	556	186	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	689	556	186	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	692	556	186	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	689	556	186	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=173;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	438	160	54	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	438	160	54	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	812	-	-	-	-	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=60;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	292	160	54	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	438	160	54	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	356	277	93	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	64	-	-	-	-	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1469;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=106;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	806	439	147	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	689	439	147	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	438	79	27	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	438	79	27	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	438	79	27	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	692	439	147	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	746	439	147	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	689	439	147	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
406601	17:7675056-7675056	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	699	439	147	D/N	Gat/Aat	rs1060501206,COSV52677055,COSV52701211,COSV53135912	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	697	555	185	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	555	555	185	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	555	555	185	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	688	555	185	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	691	555	185	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	688	555	185	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=172;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	437	159	53	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	437	159	53	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	811	-	-	-	-	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=59;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	291	159	53	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	437	159	53	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	355	276	92	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	63	-	-	-	-	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1470;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=105;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	805	438	146	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	688	438	146	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	437	78	26	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	437	78	26	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	437	78	26	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	691	438	146	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	745	438	146	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	688	438	146	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1748280	17:7675057-7675057	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	698	438	146	S/R	agC/agG	COSV52661660,COSV52701195,COSV52772909	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	697	555	185	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	555	555	185	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	555	555	185	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	688	555	185	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	691	555	185	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	688	555	185	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=172;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	437	159	53	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	437	159	53	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	811	-	-	-	-	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=59;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	291	159	53	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	437	159	53	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	355	276	92	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	63	-	-	-	-	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1470;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=105;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	805	438	146	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	688	438	146	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	437	78	26	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	437	78	26	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	437	78	26	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	691	438	146	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	745	438	146	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	688	438	146	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184650	17:7675057-7675057	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	698	438	146	S	agC/agT	rs367560109,COSV52661660,COSV52701195,COSV52772909	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	691	549	183	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	549	549	183	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	549	549	183	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	682	549	183	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	685	549	183	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	682	549	183	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=166;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	431	153	51	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	431	153	51	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	805	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=53;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	285	153	51	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	431	153	51	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	349	270	90	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	57	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1476;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=99;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	799	432	144	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	682	432	144	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	431	72	24	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	431	72	24	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	431	72	24	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	685	432	144	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	739	432	144	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	682	432	144	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1535014	17:7675063-7675063	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	692	432	144	S	tcA/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	691	549	183	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	549	549	183	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	549	549	183	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	682	549	183	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	685	549	183	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	682	549	183	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369559	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=166;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	431	153	51	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	431	153	51	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	805	-	-	-	-	rs1597369559	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369559	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=53;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	285	153	51	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	431	153	51	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	349	270	90	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	57	-	-	-	-	rs1597369559	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597369559	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1476;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369559	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=99;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	799	432	144	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	682	432	144	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	431	72	24	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	431	72	24	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	431	72	24	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	685	432	144	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	739	432	144	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	682	432	144	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762808	17:7675063-7675063	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	692	432	144	S	tcA/tcG	rs1597369559	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	685	543	181	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	543	543	181	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	543	543	181	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	676	543	181	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	679	543	181	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	676	543	181	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659582,COSV52809080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=160;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	425	147	49	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	425	147	49	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	799	-	-	-	-	rs876659582,COSV52809080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659582,COSV52809080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=47;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	279	147	49	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	425	147	49	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	343	264	88	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	51	-	-	-	-	rs876659582,COSV52809080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659582,COSV52809080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1482;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659582,COSV52809080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=93;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	793	426	142	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	676	426	142	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	425	66	22	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	425	66	22	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	425	66	22	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	679	426	142	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	733	426	142	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	676	426	142	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232142	17:7675069-7675069	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	686	426	142	R	cgC/cgT	rs876659582,COSV52809080	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	679	537	179	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	537	537	179	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	537	537	179	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	670	537	179	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	673	537	179	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	670	537	179	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=154;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	419	141	47	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	419	141	47	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	793	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=41;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	273	141	47	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	419	141	47	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	337	258	86	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	45	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1488;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=87;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	787	420	140	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	670	420	140	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	419	60	20	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	419	60	20	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	419	60	20	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	673	420	140	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	727	420	140	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	670	420	140	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
234055	17:7675075-7675075	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	680	420	140	H	caT/caC	rs876660821,CM0910925,COSV52669519,COSV52673406,COSV53016879	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	676	534	178	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	534	534	178	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	534	534	178	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	667	534	178	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	670	534	178	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	667	534	178	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=151;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	416	138	46	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	416	138	46	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	790	-	-	-	-	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=38;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	270	138	46	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	416	138	46	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	334	255	85	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	42	-	-	-	-	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1491;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=84;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	784	417	139	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	667	417	139	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	416	57	19	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	416	57	19	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	416	57	19	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	670	417	139	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	724	417	139	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	667	417	139	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
485035	17:7675078-7675078	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	677	417	139	H	caC/caT	rs1555526001,CM1313554,COSV52741277,COSV53120340,COSV53165113,COSV53624003	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1,1;PHENO=1,1,1,1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	673	531	177	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	531	531	177	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	531	531	177	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	664	531	177	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	667	531	177	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	664	531	177	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53050504,COSV53086977,COSV53135228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=148;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	413	135	45	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	413	135	45	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	787	-	-	-	-	COSV53050504,COSV53086977,COSV53135228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53050504,COSV53086977,COSV53135228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=35;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	267	135	45	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	413	135	45	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	331	252	84	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	39	-	-	-	-	COSV53050504,COSV53086977,COSV53135228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53050504,COSV53086977,COSV53135228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1494;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53050504,COSV53086977,COSV53135228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=81;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	781	414	138	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	664	414	138	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	413	54	18	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	413	54	18	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	413	54	18	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	667	414	138	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	721	414	138	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	664	414	138	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1171072	17:7675081-7675081	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	674	414	138	P	ccC/ccT	COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	673	531	177	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	531	531	177	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	531	531	177	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	664	531	177	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	667	531	177	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	664	531	177	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=148;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	413	135	45	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	413	135	45	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	787	-	-	-	-	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=35;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	267	135	45	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	413	135	45	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	331	252	84	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	39	-	-	-	-	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1494;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=81;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	781	414	138	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	664	414	138	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	413	54	18	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	413	54	18	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	413	54	18	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	667	414	138	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	721	414	138	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	664	414	138	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825645	17:7675081-7675081	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	674	414	138	P	ccC/ccG	rs1597369785,COSV53050504,COSV53086977,COSV53135228	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	667	525	175	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	525	525	175	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	525	525	175	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	658	525	175	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	661	525	175	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	658	525	175	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs976002907,COSV52773014,COSV52815137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=142;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	407	129	43	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	407	129	43	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	781	-	-	-	-	rs976002907,COSV52773014,COSV52815137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs976002907,COSV52773014,COSV52815137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=29;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	261	129	43	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	407	129	43	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	325	246	82	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	33	-	-	-	-	rs976002907,COSV52773014,COSV52815137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs976002907,COSV52773014,COSV52815137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1500;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs976002907,COSV52773014,COSV52815137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=75;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	775	408	136	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	658	408	136	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	407	48	16	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	407	48	16	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	407	48	16	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	661	408	136	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	715	408	136	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	658	408	136	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1527986	17:7675087-7675087	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	668	408	136	R	cgC/cgT	rs976002907,COSV52773014,COSV52815137	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	663	521	174	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	521	521	174	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	521	521	174	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	654	521	174	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	657	521	174	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	654	521	174	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=138;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	403	125	42	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	403	125	42	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	777	-	-	-	-	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=25;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	257	125	42	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	403	125	42	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	321	242	81	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	29	-	-	-	-	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1504;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=71;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	771	404	135	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	654	404	135	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	403	44	15	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	403	44	15	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	403	44	15	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	657	404	135	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	711	404	135	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	654	404	135	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
423887	17:7675091-7675091	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	664	404	135	R/K	aGg/aAg	rs1064796681,COSV52688730,COSV52965095,COSV53163634	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	661	519	173	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	519	519	173	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	519	519	173	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	652	519	173	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	655	519	173	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	652	519	173	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=136;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	401	123	41	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	401	123	41	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	775	-	-	-	-	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=23;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	255	123	41	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	401	123	41	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	319	240	80	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	27	-	-	-	-	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1506;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=69;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	769	402	134	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	652	402	134	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	401	42	14	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	401	42	14	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	401	42	14	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	655	402	134	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	709	402	134	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	652	402	134	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1670954	17:7675093-7675093	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	662	402	134	V	gtG/gtC	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	661	519	173	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	519	519	173	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	519	519	173	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	652	519	173	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	655	519	173	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	652	519	173	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=136;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	401	123	41	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	401	123	41	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	775	-	-	-	-	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=23;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	255	123	41	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	401	123	41	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	319	240	80	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	27	-	-	-	-	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1506;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=69;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	769	402	134	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	652	402	134	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	401	42	14	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	401	42	14	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	401	42	14	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	655	402	134	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	709	402	134	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	652	402	134	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1745995	17:7675093-7675093	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	662	402	134	V	gtG/gtT	COSV52729041,COSV52838647,COSV53229497,COSV53349805	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	658	516	172	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	516	516	172	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	516	516	172	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	649	516	172	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	652	516	172	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	649	516	172	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=133;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	398	120	40	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	398	120	40	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	772	-	-	-	-	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=20;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	252	120	40	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	398	120	40	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	316	237	79	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	24	-	-	-	-	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1509;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=66;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	766	399	133	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	649	399	133	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	398	39	13	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	398	39	13	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	398	39	13	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	652	399	133	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	706	399	133	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	649	399	133	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1618385	17:7675096-7675096	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	659	399	133	V	gtT/gtC	rs749309577,COSV52979114,COSV52979162,COSV53164017	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	655	513	171	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	513	513	171	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	513	513	171	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	646	513	171	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	649	513	171	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	646	513	171	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=130;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	395	117	39	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	395	117	39	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	769	-	-	-	-	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=17;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	249	117	39	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	395	117	39	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	313	234	78	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	21	-	-	-	-	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1512;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=63;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	763	396	132	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	646	396	132	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	395	36	12	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	395	36	12	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	395	36	12	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	649	396	132	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	703	396	132	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	646	396	132	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
480757	17:7675099-7675099	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	656	396	132	E	gaG/gaA	rs1555526078,COSV53017045,COSV53017212,COSV53135136	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	652	510	170	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	510	510	170	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	510	510	170	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	643	510	170	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	646	510	170	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	643	510	170	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=127;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	392	114	38	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	392	114	38	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	766	-	-	-	-	COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	246	114	38	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	392	114	38	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	310	231	77	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	18	-	-	-	-	COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1515;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=60;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	760	393	131	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	643	393	131	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	392	33	11	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	392	33	11	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	392	33	11	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	646	393	131	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	700	393	131	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	643	393	131	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1745402	17:7675102-7675102	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	653	393	131	T	acG/acC	COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	652	510	170	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	510	510	170	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	510	510	170	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	643	510	170	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	646	510	170	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	643	510	170	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=127;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	392	114	38	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	392	114	38	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	766	-	-	-	-	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	246	114	38	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	392	114	38	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	310	231	77	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	18	-	-	-	-	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1515;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=60;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	760	393	131	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	643	393	131	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	392	33	11	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	392	33	11	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	392	33	11	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	646	393	131	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	700	393	131	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	643	393	131	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184717	17:7675102-7675102	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	653	393	131	T	acG/acA	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	652	510	170	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	510	510	170	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	510	510	170	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	643	510	170	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	646	510	170	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	643	510	170	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=127;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	392	114	38	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	392	114	38	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	766	-	-	-	-	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=14;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	246	114	38	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	392	114	38	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	310	231	77	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	18	-	-	-	-	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1515;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=60;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	760	393	131	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	643	393	131	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	392	33	11	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	392	33	11	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	392	33	11	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	646	393	131	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	700	393	131	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	643	393	131	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825455	17:7675102-7675102	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	653	393	131	T	acG/acT	rs757544615,COSV52796495,COSV52850121,COSV53624945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	646	504	168	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	504	504	168	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	504	504	168	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	637	504	168	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	640	504	168	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	637	504	168	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=121;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	386	108	36	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	386	108	36	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	760	-	-	-	-	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=8;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	240	108	36	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	386	108	36	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	304	225	75	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	12	-	-	-	-	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1521;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=54;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	754	387	129	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	637	387	129	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	386	27	9	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	386	27	9	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	386	27	9	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	640	387	129	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	694	387	129	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	637	387	129	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
220778	17:7675108-7675108	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	647	387	129	H	caC/caT	rs746293837,COSV105029428,COSV52761294,COSV52774171,COSV53097694	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	643	501	167	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	501	501	167	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	501	501	167	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	634	501	167	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	637	501	167	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	634	501	167	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=118;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	383	105	35	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	383	105	35	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	757	-	-	-	-	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	237	105	35	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	383	105	35	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	301	222	74	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	9	-	-	-	-	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1524;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=51;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	751	384	128	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	634	384	128	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	383	24	8	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	383	24	8	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	383	24	8	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	637	384	128	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	691	384	128	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	634	384	128	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1744819	17:7675111-7675111	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	644	384	128	Q	caG/caA	COSV52701014,COSV53108662,COSV53327706,COSV53408532	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	640	498	166	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	498	498	166	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	498	498	166	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	631	498	166	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	634	498	166	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	631	498	166	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526098,COSV52809221,COSV53187995	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=115;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	380	102	34	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	380	102	34	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	754	-	-	-	-	rs1555526098,COSV52809221,COSV53187995	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000508793.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526098,COSV52809221,COSV53187995	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	234	102	34	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	380	102	34	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	298	219	73	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	6	-	-	-	-	rs1555526098,COSV52809221,COSV53187995	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526098,COSV52809221,COSV53187995	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1527;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526098,COSV52809221,COSV53187995	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=48;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	748	381	127	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	631	381	127	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	380	21	7	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	380	21	7	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	380	21	7	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	634	381	127	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	688	381	127	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	631	381	127	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
492578	17:7675114-7675114	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	641	381	127	S	tcA/tcG	rs1555526098,COSV52809221,COSV53187995	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	635	493	165	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	493	493	165	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	493	493	165	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	626	493	165	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	629	493	165	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	626	493	165	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=110;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000504290.5	Transcript	missense_variant	375	97	33	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000504937.5	Transcript	missense_variant	375	97	33	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	749	-	-	-	-	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	631	493	165	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000509690.5	Transcript	missense_variant	229	97	33	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000510385.5	Transcript	missense_variant	375	97	33	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	293	214	72	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000574684.1	Transcript	non_coding_transcript_exon_variant	1	-	-	-	-	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;EXON=1/2;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1532;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=43;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	743	376	126	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	626	376	126	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000610623.4	Transcript	missense_variant	375	16	6	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000618944.4	Transcript	missense_variant	375	16	6	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000619186.4	Transcript	missense_variant	375	16	6	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	629	376	126	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	683	376	126	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	626	376	126	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
482232	17:7675119-7675119	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	636	376	126	Q/K	Cag/Aag	rs730882001,CM1617861,COSV52677910,COSV52844585,COSV53637782	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	634	492	164	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	492	492	164	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	492	492	164	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	625	492	164	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	628	492	164	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	625	492	164	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=109;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	374	96	32	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	374	96	32	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	748	-	-	-	-	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	630	492	164	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	228	96	32	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	374	96	32	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	292	213	71	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1533;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=42;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	742	375	125	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	625	375	125	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	374	15	5	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	374	15	5	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	374	15	5	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	628	375	125	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	682	375	125	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	625	375	125	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
485026	17:7675120-7675120	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	635	375	125	K	aaG/aaA	rs1131691034,COSV53165155,COSV53219732,COSV53700637	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	625	483	161	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	483	483	161	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	483	483	161	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	616	483	161	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	619	483	161	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	616	483	161	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523101,COSV53038078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=100;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	365	87	29	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	365	87	29	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	739	-	-	-	-	rs1057523101,COSV53038078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	621	483	161	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	219	87	29	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	365	87	29	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	283	204	68	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523101,COSV53038078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523101,COSV53038078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1542;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057523101,COSV53038078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=33;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	733	366	122	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	616	366	122	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000610623.4	Transcript	synonymous_variant	365	6	2	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000618944.4	Transcript	synonymous_variant	365	6	2	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000619186.4	Transcript	synonymous_variant	365	6	2	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	619	366	122	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	673	366	122	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	616	366	122	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
388419	17:7675129-7675129	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	626	366	122	A	gcC/gcA	rs1057523101,COSV53038078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	619	477	159	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	477	477	159	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	477	477	159	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	610	477	159	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	613	477	159	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	610	477	159	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057521842,COSV52713618	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=94;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	359	81	27	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	359	81	27	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	733	-	-	-	-	rs1057521842,COSV52713618	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	615	477	159	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	213	81	27	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	359	81	27	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	277	198	66	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057521842,COSV52713618	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=16;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057521842,COSV52713618	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1548;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057521842,COSV52713618	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=27;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	727	360	120	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	610	360	120	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	359	-	-	-	-	rs1057521842,COSV52713618	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	359	-	-	-	-	rs1057521842,COSV52713618	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	359	-	-	-	-	rs1057521842,COSV52713618	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	613	360	120	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	667	360	120	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	610	360	120	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
384065	17:7675135-7675135	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	620	360	120	A	gcC/gcT	rs1057521842,COSV52713618	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	616	474	158	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	474	474	158	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	474	474	158	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	607	474	158	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	610	474	158	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	607	474	158	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=91;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	356	78	26	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	356	78	26	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	730	-	-	-	-	COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	612	474	158	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	210	78	26	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	356	78	26	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	274	195	65	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=19;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1551;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=24;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	724	357	119	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	607	357	119	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	356	-	-	-	-	COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	356	-	-	-	-	COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	356	-	-	-	-	COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	610	357	119	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	664	357	119	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	607	357	119	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1561272	17:7675138-7675138	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	617	357	119	R	cgC/cgA	COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	616	474	158	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	474	474	158	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	474	474	158	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	607	474	158	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	610	474	158	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	607	474	158	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=91;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	356	78	26	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	356	78	26	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	730	-	-	-	-	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	612	474	158	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	210	78	26	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	356	78	26	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	274	195	65	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=19;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1551;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=24;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	724	357	119	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	607	357	119	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	356	-	-	-	-	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	356	-	-	-	-	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	356	-	-	-	-	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	610	357	119	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	664	357	119	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	607	357	119	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184042	17:7675138-7675138	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	617	357	119	R	cgC/cgT	rs139200646,COSV52676878,COSV52677767,COSV53396026	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	613	471	157	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	471	471	157	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	471	471	157	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	604	471	157	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	607	471	157	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	604	471	157	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=88;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	353	75	25	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	353	75	25	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	727	-	-	-	-	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	609	471	157	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	207	75	25	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	353	75	25	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	271	192	64	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=22;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1554;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=21;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	721	354	118	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	604	354	118	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	353	-	-	-	-	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	353	-	-	-	-	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	353	-	-	-	-	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	607	354	118	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	661	354	118	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	604	354	118	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
386420	17:7675141-7675141	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	614	354	118	V	gtC/gtA	rs1057522496,COSV52921244,COSV52942938,COSV53124823	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	610	468	156	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	468	468	156	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	468	468	156	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	601	468	156	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	604	468	156	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	601	468	156	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=85;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	350	72	24	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	350	72	24	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	724	-	-	-	-	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	606	468	156	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	204	72	24	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	350	72	24	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	268	189	63	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=25;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1557;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=18;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	718	351	117	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	601	351	117	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	350	-	-	-	-	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	350	-	-	-	-	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	350	-	-	-	-	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	604	351	117	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	658	351	117	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	601	351	117	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
183945	17:7675144-7675144	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	611	351	117	R	cgC/cgT	rs761222871,COSV52675486,COSV53198467,COSV53663860	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	607	465	155	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	465	465	155	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	465	465	155	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	598	465	155	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	601	465	155	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	598	465	155	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=82;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	347	69	23	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	347	69	23	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	721	-	-	-	-	COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	603	465	155	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	201	69	23	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	347	69	23	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	265	186	62	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=28;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1560;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=15;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	715	348	116	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	598	348	116	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	347	-	-	-	-	COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	347	-	-	-	-	COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	347	-	-	-	-	COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	601	348	116	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	655	348	116	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	598	348	116	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151516	17:7675147-7675147	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	608	348	116	T	acC/acT	COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	607	465	155	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	465	465	155	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	465	465	155	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	598	465	155	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	601	465	155	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	598	465	155	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202992,COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=82;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	347	69	23	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	347	69	23	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	721	-	-	-	-	rs786202992,COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	603	465	155	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	201	69	23	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	347	69	23	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	265	186	62	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202992,COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=28;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786202992,COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1560;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs786202992,COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=15;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	715	348	116	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	598	348	116	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	347	-	-	-	-	rs786202992,COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	347	-	-	-	-	rs786202992,COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	347	-	-	-	-	rs786202992,COSV52969178,COSV53050162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	601	348	116	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	655	348	116	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	598	348	116	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
186490	17:7675147-7675147	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	608	348	116	T	acC/acA	rs786202992,COSV52969178,COSV53050162	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	604	462	154	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	462	462	154	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	462	462	154	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	595	462	154	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	598	462	154	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	595	462	154	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=79;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	344	66	22	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	344	66	22	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	718	-	-	-	-	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	600	462	154	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	198	66	22	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	344	66	22	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	262	183	61	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=31;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1563;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=12;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	712	345	115	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	595	345	115	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	344	-	-	-	-	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	344	-	-	-	-	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	344	-	-	-	-	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	598	345	115	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	652	345	115	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	595	345	115	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
133285	17:7675150-7675150	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	605	345	115	G	ggC/ggT	rs137852793,COSV52728527,COSV52892008,COSV53120332	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,not_provided;SOMATIC=0,1,1,1;PHENO=1,1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	601	459	153	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	459	459	153	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	459	459	153	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	592	459	153	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	595	459	153	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	592	459	153	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661116,COSV52700360,COSV52751929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=76;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	341	63	21	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	341	63	21	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	715	-	-	-	-	rs72661116,COSV52700360,COSV52751929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	597	459	153	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	195	63	21	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	341	63	21	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	259	180	60	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs72661116,COSV52700360,COSV52751929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=34;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs72661116,COSV52700360,COSV52751929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1566;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs72661116,COSV52700360,COSV52751929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=9;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	709	342	114	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	592	342	114	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	341	-	-	-	-	rs72661116,COSV52700360,COSV52751929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	341	-	-	-	-	rs72661116,COSV52700360,COSV52751929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	341	-	-	-	-	rs72661116,COSV52700360,COSV52751929	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	595	342	114	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	649	342	114	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	592	342	114	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
230629	17:7675153-7675153	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	602	342	114	P	ccC/ccT	rs72661116,COSV52700360,COSV52751929	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	598	456	152	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	456	456	152	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	456	456	152	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	589	456	152	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	592	456	152	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	589	456	152	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=73;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	338	60	20	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	338	60	20	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	712	-	-	-	-	COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	594	456	152	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	192	60	20	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	338	60	20	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	256	177	59	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=37;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1569;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	706	339	113	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	589	339	113	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	338	-	-	-	-	COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	338	-	-	-	-	COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	338	-	-	-	-	COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	592	339	113	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	646	339	113	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	589	339	113	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1741557	17:7675156-7675156	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	599	339	113	P	ccG/ccT	COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	598	456	152	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	456	456	152	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	456	456	152	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	589	456	152	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	592	456	152	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	589	456	152	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=73;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	338	60	20	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	338	60	20	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	712	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	594	456	152	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	192	60	20	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	338	60	20	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	256	177	59	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=37;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1569;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	706	339	113	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	589	339	113	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	338	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	338	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	338	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	592	339	113	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	646	339	113	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	589	339	113	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
231994	17:7675156-7675156	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	599	339	113	P	ccG/ccA	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	598	456	152	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	456	456	152	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	456	456	152	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	589	456	152	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	592	456	152	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	589	456	152	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=73;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	338	60	20	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	338	60	20	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	712	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	594	456	152	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	192	60	20	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	338	60	20	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	256	177	59	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=37;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1569;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	706	339	113	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	589	339	113	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	338	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	338	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	338	-	-	-	-	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	592	339	113	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	646	339	113	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	589	339	113	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
825009	17:7675156-7675156	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	599	339	113	P	ccG/ccC	rs876659481,COSV52765928,COSV52978254,COSV53086786	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	595	453	151	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	453	453	151	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	453	453	151	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	586	453	151	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	589	453	151	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	586	453	151	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52700998,COSV52772047,COSV53605873	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=70;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	335	57	19	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	335	57	19	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	709	-	-	-	-	COSV52700998,COSV52772047,COSV53605873	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	591	453	151	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	189	57	19	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	335	57	19	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	253	174	58	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52700998,COSV52772047,COSV53605873	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=40;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52700998,COSV52772047,COSV53605873	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1572;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000604348.5	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52700998,COSV52772047,COSV53605873	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	703	336	112	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	586	336	112	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	335	-	-	-	-	COSV52700998,COSV52772047,COSV53605873	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	335	-	-	-	-	COSV52700998,COSV52772047,COSV53605873	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	335	-	-	-	-	COSV52700998,COSV52772047,COSV53605873	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	589	336	112	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	643	336	112	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	586	336	112	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1148159	17:7675159-7675159	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	596	336	112	P	ccC/ccT	COSV52700998,COSV52772047,COSV53605873	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	592	450	150	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	450	450	150	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	450	450	150	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	583	450	150	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	586	450	150	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	583	450	150	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=67;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	332	54	18	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	332	54	18	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	706	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	588	450	150	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	186	54	18	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	332	54	18	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	250	171	57	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=43;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1575;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	568	429	143	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	700	333	111	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	583	333	111	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	332	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	332	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	332	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	586	333	111	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	640	333	111	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	583	333	111	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
215763	17:7675162-7675162	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	593	333	111	T	acA/acG	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	592	450	150	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	450	450	150	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	450	450	150	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	583	450	150	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	586	450	150	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	583	450	150	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=67;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	332	54	18	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	332	54	18	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	706	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	588	450	150	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	186	54	18	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	332	54	18	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	250	171	57	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=43;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1575;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	568	429	143	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	700	333	111	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	583	333	111	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	332	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	332	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	332	-	-	-	-	rs754020850,CD044990,COSV52926447	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	586	333	111	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	640	333	111	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	583	333	111	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
516982	17:7675162-7675162	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	593	333	111	T	acA/acC	rs754020850,CD044990,COSV52926447	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	589	447	149	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	447	447	149	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	447	447	149	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	580	447	149	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	583	447	149	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	580	447	149	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52772756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=64;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	329	51	17	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	329	51	17	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	703	-	-	-	-	COSV52772756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	585	447	149	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	183	51	17	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	329	51	17	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	247	168	56	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52772756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=46;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52772756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1578;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	565	426	142	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	697	330	110	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	580	330	110	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	329	-	-	-	-	COSV52772756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	329	-	-	-	-	COSV52772756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	329	-	-	-	-	COSV52772756	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	583	330	110	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	637	330	110	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	580	330	110	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1639265	17:7675165-7675165	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	590	330	110	S	tcC/tcT	COSV52772756	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	575	433	145	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	433	433	145	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	433	433	145	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	566	433	145	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	569	433	145	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	566	433	145	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=50;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	315	37	13	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	315	37	13	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	689	-	-	-	-	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	571	433	145	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	169	37	13	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	315	37	13	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	233	154	52	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=60;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1592;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	551	412	138	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	683	316	106	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	566	316	106	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	315	-	-	-	-	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	315	-	-	-	-	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	315	-	-	-	-	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	569	316	106	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	623	316	106	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	566	316	106	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
187696	17:7675179-7675179	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	576	316	106	L	Ctg/Ttg	rs786203928,COSV52773400,COSV52783731,COSV53685276	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	574	432	144	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	432	432	144	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	432	432	144	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	565	432	144	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	568	432	144	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	565	432	144	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=49;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	314	36	12	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	314	36	12	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	688	-	-	-	-	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	570	432	144	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	168	36	12	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	314	36	12	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	232	153	51	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=61;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1593;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	550	411	137	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	682	315	105	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	565	315	105	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	314	-	-	-	-	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	314	-	-	-	-	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	314	-	-	-	-	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	568	315	105	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	622	315	105	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	565	315	105	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
184357	17:7675180-7675180	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	575	315	105	Q	caG/caA	rs786201419,COSV52676427,COSV52842986,COSV53108952	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	556	414	138	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	414	414	138	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	414	414	138	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	547	414	138	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	550	414	138	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	547	414	138	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526254,COSV52677977	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=31;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	296	18	6	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	296	18	6	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	670	-	-	-	-	rs1555526254,COSV52677977	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	552	414	138	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	150	18	6	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	296	18	6	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	214	135	45	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526254,COSV52677977	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=79;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526254,COSV52677977	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1611;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	532	393	131	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	664	297	99	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	547	297	99	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	296	-	-	-	-	rs1555526254,COSV52677977	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	296	-	-	-	-	rs1555526254,COSV52677977	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	296	-	-	-	-	rs1555526254,COSV52677977	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	550	297	99	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	604	297	99	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	547	297	99	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
482234	17:7675198-7675198	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	557	297	99	A	gcC/gcT	rs1555526254,COSV52677977	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	553	411	137	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	411	411	137	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	411	411	137	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	544	411	137	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	547	411	137	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	544	411	137	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=28;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	293	15	5	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	293	15	5	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	667	-	-	-	-	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	549	411	137	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	147	15	5	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	293	15	5	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	211	132	44	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=82;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1614;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	529	390	130	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	661	294	98	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	544	294	98	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	293	-	-	-	-	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	293	-	-	-	-	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	293	-	-	-	-	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	547	294	98	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	601	294	98	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	544	294	98	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
233916	17:7675201-7675201	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	554	294	98	L	ctG/ctC	rs876660731,COSV52676837,COSV52688445,COSV52773610	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	551	409	137	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	409	409	137	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	409	409	137	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	542	409	137	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	545	409	137	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	542	409	137	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=26;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	291	13	5	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	291	13	5	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	665	-	-	-	-	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	547	409	137	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	145	13	5	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	291	13	5	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	209	130	44	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=84;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1616;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	527	388	130	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	659	292	98	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	542	292	98	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	291	-	-	-	-	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	291	-	-	-	-	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	291	-	-	-	-	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	545	292	98	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	599	292	98	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	542	292	98	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1737807	17:7675203-7675203	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	552	292	98	L	Ctg/Ttg	COSV52815191,COSV52864264,COSV52994461,COSV53153059	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	550	408	136	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	408	408	136	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	408	408	136	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	541	408	136	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	544	408	136	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	541	408	136	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=25;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	290	12	4	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	290	12	4	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	664	-	-	-	-	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	546	408	136	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	144	12	4	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	290	12	4	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	208	129	43	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=85;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1617;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	526	387	129	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	658	291	97	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	541	291	97	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	290	-	-	-	-	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	290	-	-	-	-	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	290	-	-	-	-	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	544	291	97	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	598	291	97	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	541	291	97	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
185409	17:7675204-7675204	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	551	291	97	Q	caA/caG	rs758781593,CM064342,COSV52979889,COSV52987518,COSV52988005	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	547	405	135	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	405	405	135	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	405	405	135	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	538	405	135	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	541	405	135	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	538	405	135	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=22;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	287	9	3	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	287	9	3	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	661	-	-	-	-	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	543	405	135	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	141	9	3	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	287	9	3	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	205	126	42	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=88;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1620;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	523	384	128	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	655	288	96	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	538	288	96	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	287	-	-	-	-	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	287	-	-	-	-	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	287	-	-	-	-	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	541	288	96	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	595	288	96	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	538	288	96	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
480744	17:7675207-7675207	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	548	288	96	C	tgC/tgT	rs1057519976,COSV52665429,COSV52669330,COSV52682693,COSV52815283	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	544	402	134	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	402	402	134	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	402	402	134	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	535	402	134	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	538	402	134	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	535	402	134	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=19;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000504290.5	Transcript	synonymous_variant	284	6	2	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000504937.5	Transcript	synonymous_variant	284	6	2	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	658	-	-	-	-	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	540	402	134	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000509690.5	Transcript	synonymous_variant	138	6	2	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000510385.5	Transcript	synonymous_variant	284	6	2	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	202	123	41	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=91;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1623;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	520	381	127	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	652	285	95	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	535	285	95	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	284	-	-	-	-	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	284	-	-	-	-	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	284	-	-	-	-	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	538	285	95	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	592	285	95	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	535	285	95	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
492577	17:7675210-7675210	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	545	285	95	F	ttT/ttC	rs1555526278,COSV52723236,COSV52814502,COSV52902300	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	535	393	131	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	393	393	131	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	393	393	131	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	526	393	131	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	529	393	131	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	526	393	131	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=10;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	275	-	-	-	-	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	275	-	-	-	-	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	649	-	-	-	-	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	531	393	131	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	129	-	-	-	-	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	275	-	-	-	-	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	193	114	38	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=100;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1632;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	643	276	92	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	526	276	92	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	275	-	-	-	-	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	275	-	-	-	-	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	275	-	-	-	-	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	529	276	92	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	583	276	92	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	526	276	92	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
922981	17:7675219-7675219	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	536	276	92	N	aaC/aaT	COSV52891063,COSV52938317,COSV53696738,COSV53770947	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	532	390	130	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	390	390	130	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	390	390	130	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	523	390	130	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	526	390	130	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	523	390	130	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs781537596,COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=7;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	272	-	-	-	-	rs781537596,COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	272	-	-	-	-	rs781537596,COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	646	-	-	-	-	rs781537596,COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	528	390	130	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	126	-	-	-	-	rs781537596,COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	272	-	-	-	-	rs781537596,COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	190	111	37	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs781537596,COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=103;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs781537596,COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1635;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	640	273	91	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	523	273	91	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	272	-	-	-	-	rs781537596,COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	272	-	-	-	-	rs781537596,COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	272	-	-	-	-	rs781537596,COSV52782624	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	526	273	91	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	580	273	91	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	523	273	91	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186498	17:7675222-7675222	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	533	273	91	L	ctC/ctT	rs781537596,COSV52782624	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	529	387	129	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	387	387	129	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	387	387	129	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	520	387	129	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	523	387	129	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	520	387	129	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	269	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	269	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	643	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	525	387	129	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	123	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	269	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	187	108	36	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=106;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1638;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	637	270	90	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	520	270	90	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	269	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	269	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	269	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	523	270	90	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	577	270	90	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	520	270	90	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735782	17:7675225-7675225	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	530	270	90	A	gcC/gcT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	528	386	129	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	386	386	129	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	386	386	129	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	519	386	129	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	522	386	129	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	519	386	129	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	268	-	-	-	-	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	268	-	-	-	-	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	642	-	-	-	-	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	524	386	129	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	122	-	-	-	-	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	268	-	-	-	-	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	186	107	36	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=107;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1639;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	636	269	90	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	519	269	90	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	268	-	-	-	-	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	268	-	-	-	-	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	268	-	-	-	-	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	522	269	90	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	576	269	90	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	519	269	90	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735669	17:7675226-7675226	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	529	269	90	A/D	gCc/gAc	COSV52815126,COSV52828986,COSV53008878,COSV53606125	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	526	384	128	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	384	384	128	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	384	384	128	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	517	384	128	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	520	384	128	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	517	384	128	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	266	-	-	-	-	COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	266	-	-	-	-	COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	640	-	-	-	-	COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	522	384	128	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	120	-	-	-	-	COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	266	-	-	-	-	COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	184	105	35	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=109;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1641;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	634	267	89	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	517	267	89	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	266	-	-	-	-	COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	266	-	-	-	-	COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	266	-	-	-	-	COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	520	267	89	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	574	267	89	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	517	267	89	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735514	17:7675228-7675228	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	527	267	89	P	ccT/ccA	COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	526	384	128	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	384	384	128	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	384	384	128	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	517	384	128	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	520	384	128	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	517	384	128	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000503591.1	Transcript	downstream_gene_variant	-	-	-	-	-	rs1555526324,COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	266	-	-	-	-	rs1555526324,COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	266	-	-	-	-	rs1555526324,COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	640	-	-	-	-	rs1555526324,COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	522	384	128	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	120	-	-	-	-	rs1555526324,COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	266	-	-	-	-	rs1555526324,COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	184	105	35	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526324,COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=109;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526324,COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1641;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	634	267	89	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	517	267	89	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	266	-	-	-	-	rs1555526324,COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	266	-	-	-	-	rs1555526324,COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	266	-	-	-	-	rs1555526324,COSV53527927	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	520	267	89	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	574	267	89	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	517	267	89	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
480752	17:7675228-7675228	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	527	267	89	P	ccT/ccC	rs1555526324,COSV53527927	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	523	381	127	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	381	381	127	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	381	381	127	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	514	381	127	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	517	381	127	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	514	381	127	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	563	381	127	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	263	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	263	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	637	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	519	381	127	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	117	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	263	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	181	102	34	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=112;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1644;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	631	264	88	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	514	264	88	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	263	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	263	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	263	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	517	264	88	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	571	264	88	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	514	264	88	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1149624	17:7675231-7675231	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	524	264	88	S	tcC/tcA	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	523	381	127	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	381	381	127	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	381	381	127	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	514	381	127	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	517	381	127	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	514	381	127	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	563	381	127	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	263	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	263	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	637	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	519	381	127	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	117	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	263	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	181	102	34	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=112;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1644;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	631	264	88	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	514	264	88	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	263	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	263	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	263	-	-	-	-	COSV52979463	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	517	264	88	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	571	264	88	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	514	264	88	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1670830	17:7675231-7675231	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	524	264	88	S	tcC/tcT	COSV52979463	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	520	378	126	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,synonymous_variant	378	378	126	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,synonymous_variant	378	378	126	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,synonymous_variant	511	378	126	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	514	378	126	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,synonymous_variant	511	378	126	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,synonymous_variant	560	378	126	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=6/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	260	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	260	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	634	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=4/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,synonymous_variant	516	378	126	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,5_prime_UTR_variant	114	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	260	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,synonymous_variant	178	99	33	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=115;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1647;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,synonymous_variant	628	261	87	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,synonymous_variant	511	261	87	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	260	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	260	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	260	-	-	-	-	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,synonymous_variant	514	261	87	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,synonymous_variant	568	261	87	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,synonymous_variant	511	261	87	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
927004	17:7675234-7675234	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,synonymous_variant,NMD_transcript_variant	521	261	87	Y	taC/taT	CM1414507,COSV52662583,COSV52757878,COSV52964885,COSV53125652	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=5/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1,1,1,1;PHENO=1,1,1,1,1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	251	-	-	-	-	rs1555526345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	251	-	-	-	-	rs1555526345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	251	-	-	-	-	rs1555526345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=124;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1656;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1555526345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	251	-	-	-	-	rs1555526345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	251	-	-	-	-	rs1555526345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	251	-	-	-	-	rs1555526345	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
510753	17:7675243-7675243	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526345	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	250	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	250	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	250	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=125;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1657;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	250	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	250	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	250	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1143878	17:7675244-7675244	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	249	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	249	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	249	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=126;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1658;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	249	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	249	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	249	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1083713	17:7675245-7675245	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	248	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	248	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	248	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=127;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1659;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	248	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	248	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	248	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1552045	17:7675246-7675246	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1279988398,COSV52796547,COSV53388245	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	247	-	-	-	-	rs747705704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	247	-	-	-	-	rs747705704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	247	-	-	-	-	rs747705704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs747705704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=128;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs747705704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1660;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs747705704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	247	-	-	-	-	rs747705704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	247	-	-	-	-	rs747705704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	247	-	-	-	-	rs747705704	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1641773	17:7675247-7675247	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs747705704	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	245	-	-	-	-	rs2073407612,COSV53458001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	245	-	-	-	-	rs2073407612,COSV53458001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	245	-	-	-	-	rs2073407612,COSV53458001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=130;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1662;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	245	-	-	-	-	rs2073407612,COSV53458001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	245	-	-	-	-	rs2073407612,COSV53458001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	245	-	-	-	-	rs2073407612,COSV53458001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919415	17:7675249-7675249	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2073407612,COSV53458001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	244	-	-	-	-	rs2073407763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	244	-	-	-	-	rs2073407763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	244	-	-	-	-	rs2073407763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073407763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=131;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073407763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1663;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs2073407763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	244	-	-	-	-	rs2073407763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	244	-	-	-	-	rs2073407763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	244	-	-	-	-	rs2073407763	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
919358	17:7675250-7675250	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2073407763	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	242	-	-	-	-	rs1202851517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	242	-	-	-	-	rs1202851517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	242	-	-	-	-	rs1202851517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1202851517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=133;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1202851517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1665;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1202851517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	242	-	-	-	-	rs1202851517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	242	-	-	-	-	rs1202851517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	242	-	-	-	-	rs1202851517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1365790	17:7675252-7675252	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1202851517	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	240-241	-	-	-	-	rs756417643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	240-241	-	-	-	-	rs756417643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	240-241	-	-	-	-	rs756417643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs756417643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=134;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs756417643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1666;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs756417643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	240-241	-	-	-	-	rs756417643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	240-241	-	-	-	-	rs756417643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	240-241	-	-	-	-	rs756417643	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
372074	17:7675253-7675253	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs756417643	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	241	-	-	-	-	rs376713749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	241	-	-	-	-	rs376713749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000509690.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	241	-	-	-	-	rs376713749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs376713749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=134;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs376713749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1666;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs376713749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	241	-	-	-	-	rs376713749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	241	-	-	-	-	rs376713749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	241	-	-	-	-	rs376713749	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
378744	17:7675253-7675253	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs376713749	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	238-239	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	238-239	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	238-239	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=136;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1668;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	238-239	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	238-239	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	238-239	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1551064	17:7675255-7675255	AC	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	239	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	239	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	239	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=136;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1668;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	239	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	239	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	239	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
383385	17:7675255-7675255	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1057521606	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	238	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	238	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	238	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=137;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1669;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	238	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	238	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	238	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492576	17:7675256-7675256	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1483487754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	234	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	234	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	234	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=141;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1673;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	234	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	234	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	234	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1802905	17:7675260-7675260	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1481480007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	172	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	172	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	172	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=203;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1735;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	172	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	172	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	172	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670317	17:7675322-7675322	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs113530090,COSV104369759	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	167	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	167	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	167	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=208;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1740;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	167	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	167	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	167	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
440348	17:7675327-7675327	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2909430,COSV52668782	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	157	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	157	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	157	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=218;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1750;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	157	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	157	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	157	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1319321	17:7675337-7675337	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs145153611	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	141	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	141	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	141	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=234;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1766;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	141	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	141	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	141	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
670316	17:7675353-7675353	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs35850753,COSV104370796	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	133	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	133	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	133	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=242;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1774;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	133	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	133	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	133	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1245512	17:7675361-7675361	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs9895829,COSV53475599	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	99-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	99-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	99-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=275;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1807;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	99-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	99-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	99-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1213246	17:7675393-7675395	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=275;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1807;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803308	17:7675393-7675394	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	98-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	98-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	98-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=275;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1807;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	98-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	98-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	98-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803309	17:7675393-7675396	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	97-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	97-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	97-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=275;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1807;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	97-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	97-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	97-100	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
803310	17:7675393-7675397	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs5819162	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000504290.5	Transcript	5_prime_UTR_variant	97	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000504937.5	Transcript	5_prime_UTR_variant	97	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000510385.5	Transcript	5_prime_UTR_variant	97	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=278;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1810;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000610623.4	Transcript	5_prime_UTR_variant	97	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000618944.4	Transcript	5_prime_UTR_variant	97	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000619186.4	Transcript	5_prime_UTR_variant	97	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1236480	17:7675397-7675397	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs75821853	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=26;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=26;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=26;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=400;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1932;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=26;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=26;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=26;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
695142	17:7675519-7675519	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1794287,CR104657	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=483;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=483;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=483;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=857;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2389;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=483;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=483;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=483;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630624	17:7675976-7675976	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567555404,COSV52808142	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=484;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=484;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=484;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2390;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=484;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=484;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=484;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
372058	17:7675977-7675977	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs765179201,COSV53267806	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=485;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=485;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=485;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=859;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2391;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=485;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=485;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=485;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
385441	17:7675978-7675978	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs750477922	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=488;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=488;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=488;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=862;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2394;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=488;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=488;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=488;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
379461	17:7675981-7675981	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs758658664	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=489;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=489;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=489;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=863;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2395;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=489;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=489;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=489;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1614351	17:7675982-7675982	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=5/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=3/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=867;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2399;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=493;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
766673	17:7675986-7675986	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1597373333,COSV53209061	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	508	366	122	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	366	366	122	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	366	366	122	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	499	366	122	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	502	366	122	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	499	366	122	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	548	366	122	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	622	-	-	-	-	CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	504	366	122	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=884;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2416;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	505	366	122	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	616	249	83	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	499	249	83	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	502	249	83	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	556	249	83	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	499	249	83	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1135834	17:7676003-7676003	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	509	249	83	V	gtG/gtT	CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	508	366	122	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	366	366	122	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	366	366	122	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	499	366	122	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	502	366	122	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	499	366	122	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	548	366	122	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1374112390,CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1374112390,CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	622	-	-	-	-	rs1374112390,CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	504	366	122	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1374112390,CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1374112390,CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1374112390,CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1374112390,CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=884;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1374112390,CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2416;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	505	366	122	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	616	249	83	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	499	249	83	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1374112390,CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1374112390,CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1374112390,CD068497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=510;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	502	249	83	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	556	249	83	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	499	249	83	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1141459	17:7676003-7676003	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	509	249	83	V	gtG/gtA	rs1374112390,CD068497	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	506	364	122	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	364	364	122	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	364	364	122	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	497	364	122	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	500	364	122	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	497	364	122	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	546	364	122	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781495,COSV53486625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=512;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781495,COSV53486625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=512;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	620	-	-	-	-	rs587781495,COSV53486625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	502	364	122	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587781495,COSV53486625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781495,COSV53486625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=512;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587781495,COSV53486625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781495,COSV53486625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=886;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781495,COSV53486625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2418;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	503	364	122	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	614	247	83	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	497	247	83	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781495,COSV53486625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=512;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781495,COSV53486625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=512;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781495,COSV53486625	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=512;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	500	247	83	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	554	247	83	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	497	247	83	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
141101	17:7676005-7676005	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	507	247	83	V/M	Gtg/Atg	rs587781495,COSV53486625	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	505	363	121	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	363	363	121	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	363	363	121	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	496	363	121	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	499	363	121	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	496	363	121	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	545	363	121	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555531,COSV53584943	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=513;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555531,COSV53584943	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=513;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	619	-	-	-	-	rs1567555531,COSV53584943	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	501	363	121	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567555531,COSV53584943	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555531,COSV53584943	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=513;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567555531,COSV53584943	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555531,COSV53584943	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=887;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555531,COSV53584943	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2419;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	502	363	121	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	613	246	82	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	496	246	82	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555531,COSV53584943	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=513;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555531,COSV53584943	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=513;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567555531,COSV53584943	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=513;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	499	246	82	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	553	246	82	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	496	246	82	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
628118	17:7676006-7676006	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	506	246	82	S	tcT/tcG	rs1567555531,COSV53584943	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	496	354	118	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	354	354	118	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	354	354	118	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	487	354	118	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	490	354	118	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	487	354	118	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	536	354	118	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	610	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	492	354	118	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=896;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2428;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	493	354	118	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	604	237	79	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	487	237	79	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	490	237	79	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	544	237	79	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	487	237	79	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1119798	17:7676015-7676015	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	497	237	79	T	acA/acG	COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	496	354	118	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	354	354	118	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	354	354	118	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	487	354	118	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	490	354	118	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	487	354	118	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	536	354	118	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs751978853,COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs751978853,COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	610	-	-	-	-	rs751978853,COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	492	354	118	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs751978853,COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs751978853,COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs751978853,COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs751978853,COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=896;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs751978853,COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2428;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	493	354	118	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	604	237	79	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	487	237	79	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs751978853,COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs751978853,COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs751978853,COSV53220114	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	490	237	79	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	544	237	79	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	487	237	79	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184317	17:7676015-7676015	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	497	237	79	T	acA/acT	rs751978853,COSV53220114	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	493	351	117	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	351	351	117	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	351	351	117	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	484	351	117	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	487	351	117	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	484	351	117	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	533	351	117	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=525;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=525;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	607	-	-	-	-	rs876658998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	489	351	117	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876658998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=525;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs876658998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=899;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2431;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	490	351	117	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	601	234	78	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	484	234	78	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=525;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=525;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658998	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=525;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	487	234	78	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	541	234	78	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	484	234	78	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231170	17:7676018-7676018	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	494	234	78	G	ggG/ggA	rs876658998	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	490	348	116	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	348	348	116	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	348	348	116	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	481	348	116	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	484	348	116	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	481	348	116	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	530	348	116	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	604	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	486	348	116	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=902;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2434;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	487	348	116	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	598	231	77	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	481	231	77	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=528;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	484	231	77	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	538	231	77	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	481	231	77	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1160545	17:7676021-7676021	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	491	231	77	S	tcT/tcC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	487	345	115	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	345	345	115	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	345	345	115	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	478	345	115	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	481	345	115	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	478	345	115	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	527	345	115	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=531;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=531;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	601	-	-	-	-	rs1555526530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	483	345	115	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=531;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2437;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	484	345	115	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	595	228	76	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	478	228	76	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=531;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=531;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=531;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	481	228	76	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	535	228	76	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	478	228	76	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486999	17:7676024-7676024	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	488	228	76	H	caT/caC	rs1555526530	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	486	344	115	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	344	344	115	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	344	344	115	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	477	344	115	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	480	344	115	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	477	344	115	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	526	344	115	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730881996,COSV53387474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=532;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730881996,COSV53387474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=532;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	600	-	-	-	-	rs730881996,COSV53387474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	482	344	115	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs730881996,COSV53387474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730881996,COSV53387474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=532;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs730881996,COSV53387474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730881996,COSV53387474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=906;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730881996,COSV53387474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2438;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	483	344	115	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	594	227	76	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	477	227	76	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730881996,COSV53387474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=532;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730881996,COSV53387474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=532;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730881996,COSV53387474	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=532;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	480	227	76	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	534	227	76	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	477	227	76	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
182925	17:7676025-7676025	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	487	227	76	H/R	cAt/cGt	rs730881996,COSV53387474	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	478	336	112	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	336	336	112	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	336	336	112	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	469	336	112	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	472	336	112	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	469	336	112	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	518	336	112	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	592	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	474	336	112	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=914;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2446;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	475	336	112	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	586	219	73	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	469	219	73	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	472	219	73	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	526	219	73	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	469	219	73	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
231467	17:7676033-7676033	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	479	219	73	G	ggC/ggA	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	478	336	112	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	336	336	112	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	336	336	112	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	469	336	112	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	472	336	112	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	469	336	112	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	518	336	112	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	592	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	474	336	112	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=914;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2446;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	475	336	112	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	586	219	73	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	469	219	73	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659177,COSV53337795,COSV53497232	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=540;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	472	219	73	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	526	219	73	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	469	219	73	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
760514	17:7676033-7676033	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	479	219	73	G	ggC/ggG	rs876659177,COSV53337795,COSV53497232	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	473	331	111	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	331	331	111	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	331	331	111	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	464	331	111	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	467	331	111	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	464	331	111	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	513	331	111	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1403707528,COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1403707528,COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	587	-	-	-	-	rs1403707528,COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	469	331	111	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1403707528,COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1403707528,COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1403707528,COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1403707528,COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=919;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1403707528,COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2451;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	470	331	111	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	581	214	72	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	464	214	72	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1403707528,COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1403707528,COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1403707528,COSV105032054,COSV53244109	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	467	214	72	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	521	214	72	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	464	214	72	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
704964	17:7676038-7676038	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	474	214	72	L	Ctg/Ttg	rs1403707528,COSV105032054,COSV53244109	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	472	330	110	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	330	330	110	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	330	330	110	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	463	330	110	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	466	330	110	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	463	330	110	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	512	330	110	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	586	-	-	-	-	rs1060504167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	468	330	110	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1060504167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1060504167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=920;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2452;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	469	330	110	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	580	213	71	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	463	213	71	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=546;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	466	213	71	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	520	213	71	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	463	213	71	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414035	17:7676039-7676039	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	473	213	71	R	cgT/cgC	rs1060504167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	469	327	109	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	327	327	109	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	327	327	109	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	460	327	109	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	463	327	109	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	460	327	109	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	509	327	109	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586529,COSV52712716,COSV52762007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586529,COSV52712716,COSV52762007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	583	-	-	-	-	COSV104586529,COSV52712716,COSV52762007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	465	327	109	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV104586529,COSV52712716,COSV52762007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586529,COSV52712716,COSV52762007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV104586529,COSV52712716,COSV52762007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586529,COSV52712716,COSV52762007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=923;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586529,COSV52712716,COSV52762007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2455;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	466	327	109	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	577	210	70	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	460	210	70	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586529,COSV52712716,COSV52762007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586529,COSV52712716,COSV52762007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586529,COSV52712716,COSV52762007	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=549;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	463	210	70	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	517	210	70	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	460	210	70	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1729712	17:7676042-7676042	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	470	210	70	F	ttC/ttT	COSV104586529,COSV52712716,COSV52762007	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	463	321	107	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	321	321	107	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	321	321	107	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	454	321	107	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	457	321	107	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	454	321	107	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	503	321	107	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	577	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	459	321	107	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=929;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2461;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	460	321	107	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	571	204	68	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	454	204	68	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=555;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	457	204	68	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	511	204	68	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	454	204	68	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
233700	17:7676048-7676048	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	464	204	68	Y	taC/taT	rs770776262,CM154128,COSV52703111,COSV52765697,COSV53067955	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1,1,1;PHENO=1,1,1,1,1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	457	315	105	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	315	315	105	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	315	315	105	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	448	315	105	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	451	315	105	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	448	315	105	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	497	315	105	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53637914	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=561;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53637914	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=561;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	571	-	-	-	-	COSV53637914	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	453	315	105	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53637914	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53637914	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=561;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53637914	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53637914	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=935;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53637914	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2467;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	454	315	105	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	565	198	66	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	448	198	66	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53637914	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=561;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53637914	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=561;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53637914	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=561;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	451	198	66	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	505	198	66	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	448	198	66	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1728269	17:7676054-7676054	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	458	198	66	G	ggC/ggA	COSV53637914	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	454	312	104	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	312	312	104	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	312	312	104	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	445	312	104	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	448	312	104	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	445	312	104	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	494	312	104	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs745692731,COSV53017086,COSV53120104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=564;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs745692731,COSV53017086,COSV53120104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=564;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	568	-	-	-	-	rs745692731,COSV53017086,COSV53120104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	450	312	104	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs745692731,COSV53017086,COSV53120104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs745692731,COSV53017086,COSV53120104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=564;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs745692731,COSV53017086,COSV53120104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs745692731,COSV53017086,COSV53120104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=938;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs745692731,COSV53017086,COSV53120104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2470;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	451	312	104	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	562	195	65	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	445	195	65	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs745692731,COSV53017086,COSV53120104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=564;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs745692731,COSV53017086,COSV53120104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=564;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs745692731,COSV53017086,COSV53120104	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=564;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	448	195	65	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	502	195	65	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	445	195	65	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
793842	17:7676057-7676057	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	455	195	65	Q	caG/caA	rs745692731,COSV53017086,COSV53120104	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	448	306	102	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	306	306	102	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	306	306	102	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	439	306	102	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	442	306	102	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	439	306	102	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	488	306	102	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=570;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=570;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	562	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	444	306	102	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=570;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=944;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2476;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	445	306	102	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	556	189	63	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	439	189	63	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=570;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=570;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=570;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	442	189	63	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	496	189	63	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	439	189	63	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1799457	17:7676063-7676063	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	449	189	63	T	acC/acA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	442	300	100	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	300	300	100	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	300	300	100	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	433	300	100	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	436	300	100	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	433	300	100	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	482	300	100	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373952,COSV105877847,COSV53093669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=576;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373952,COSV105877847,COSV53093669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=576;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	556	-	-	-	-	rs1597373952,COSV105877847,COSV53093669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	438	300	100	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597373952,COSV105877847,COSV53093669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373952,COSV105877847,COSV53093669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=576;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597373952,COSV105877847,COSV53093669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373952,COSV105877847,COSV53093669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=950;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373952,COSV105877847,COSV53093669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2482;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	439	300	100	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	550	183	61	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	433	183	61	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373952,COSV105877847,COSV53093669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=576;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373952,COSV105877847,COSV53093669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=576;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597373952,COSV105877847,COSV53093669	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=576;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	436	183	61	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	490	183	61	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	433	183	61	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
762642	17:7676069-7676069	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	443	183	61	Q	caG/caA	rs1597373952,COSV105877847,COSV53093669	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	439	297	99	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	297	297	99	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	297	297	99	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	430	297	99	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	433	297	99	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	430	297	99	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	479	297	99	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs751494750,CD167568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=579;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs751494750,CD167568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=579;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	553	-	-	-	-	rs751494750,CD167568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	435	297	99	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs751494750,CD167568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs751494750,CD167568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=579;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs751494750,CD167568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs751494750,CD167568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=953;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs751494750,CD167568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2485;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	436	297	99	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	547	180	60	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	430	180	60	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs751494750,CD167568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=579;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs751494750,CD167568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=579;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs751494750,CD167568	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=579;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	433	180	60	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	487	180	60	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	430	180	60	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
229963	17:7676072-7676072	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	440	180	60	S	tcC/tcT	rs751494750,CD167568	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	433	291	97	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	291	291	97	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	291	291	97	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	424	291	97	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	427	291	97	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	424	291	97	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	473	291	97	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52907708,COSV53200016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=585;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52907708,COSV53200016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=585;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	547	-	-	-	-	COSV52907708,COSV53200016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	429	291	97	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52907708,COSV53200016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52907708,COSV53200016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=585;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52907708,COSV53200016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52907708,COSV53200016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=959;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52907708,COSV53200016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2491;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	430	291	97	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	541	174	58	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	424	174	58	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52907708,COSV53200016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=585;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52907708,COSV53200016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=585;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52907708,COSV53200016	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=585;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	427	174	58	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	481	174	58	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	424	174	58	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1797673	17:7676078-7676078	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	434	174	58	V	gtC/gtA	COSV52907708,COSV53200016	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	430	288	96	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	288	288	96	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	288	288	96	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	421	288	96	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	424	288	96	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	421	288	96	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	470	288	96	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	544	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	426	288	96	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=962;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2494;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	427	288	96	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	538	171	57	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	421	171	57	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	424	171	57	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	478	171	57	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	421	171	57	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1331899	17:7676081-7676081	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	431	171	57	S	tcT/tcC	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	430	288	96	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	288	288	96	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	288	288	96	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	421	288	96	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	424	288	96	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	421	288	96	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	470	288	96	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	544	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	426	288	96	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=962;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2494;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	427	288	96	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	538	171	57	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	421	171	57	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD1511154	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=588;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	424	171	57	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	478	171	57	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	421	171	57	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1797293	17:7676081-7676081	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	431	171	57	S	tcT/tcG	CD1511154	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	427	285	95	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	285	285	95	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	285	285	95	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	418	285	95	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	421	285	95	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	418	285	95	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	467	285	95	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658696,COSV104586361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=591;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658696,COSV104586361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=591;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	541	-	-	-	-	rs876658696,COSV104586361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	423	285	95	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876658696,COSV104586361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658696,COSV104586361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=591;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs876658696,COSV104586361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658696,COSV104586361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=965;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658696,COSV104586361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2497;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	424	285	95	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	535	168	56	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	418	168	56	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658696,COSV104586361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=591;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658696,COSV104586361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=591;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658696,COSV104586361	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=591;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	421	168	56	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	475	168	56	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	418	168	56	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230666	17:7676084-7676084	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	428	168	56	S	tcT/tcG	rs876658696,COSV104586361	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	424	282	94	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	282	282	94	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	282	282	94	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	415	282	94	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	418	282	94	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	415	282	94	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	464	282	94	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	538	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	420	282	94	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=968;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2500;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	421	282	94	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	532	165	55	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	415	165	55	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	418	165	55	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	472	165	55	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	415	165	55	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
233956	17:7676087-7676087	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	425	165	55	S	tcA/tcG	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	424	282	94	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	282	282	94	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	282	282	94	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	415	282	94	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	418	282	94	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	415	282	94	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	464	282	94	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	538	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	420	282	94	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=968;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2500;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	421	282	94	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	532	165	55	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	415	165	55	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs771721337,COSV99037030	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=594;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	418	165	55	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	472	165	55	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	415	165	55	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
793652	17:7676087-7676087	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	425	165	55	S	tcA/tcT	rs771721337,COSV99037030	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	423	281	94	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	281	281	94	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	281	281	94	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	414	281	94	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	417	281	94	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	414	281	94	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	463	281	94	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=595;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=595;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	537	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	419	281	94	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=595;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=969;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2501;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	420	281	94	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	531	164	55	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	414	164	55	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=595;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=595;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=595;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	417	164	55	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	471	164	55	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	414	164	55	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1796426	17:7676088-7676088	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	424	164	55	S/L	tCa/tTa	COSV52677652,COSV52734727,COSV52787469,COSV53371041	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1,1;PHENO=1,1,1,1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	421	279	93	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	279	279	93	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	279	279	93	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	412	279	93	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	415	279	93	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	412	279	93	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	461	279	93	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	535	-	-	-	-	COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	417	279	93	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2503;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	418	279	93	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	529	162	54	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	412	162	54	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	415	162	54	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	469	162	54	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	412	162	54	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1078356	17:7676090-7676090	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	422	162	54	L	ctG/ctA	COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	421	279	93	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	279	279	93	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	279	279	93	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	412	279	93	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	415	279	93	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	412	279	93	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	461	279	93	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854067,COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854067,COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	535	-	-	-	-	rs878854067,COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	417	279	93	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs878854067,COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854067,COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs878854067,COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854067,COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854067,COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2503;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	418	279	93	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	529	162	54	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	412	162	54	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854067,COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854067,COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854067,COSV53060538	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=597;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	415	162	54	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	469	162	54	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	412	162	54	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
237945	17:7676090-7676090	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	422	162	54	L	ctG/ctT	rs878854067,COSV53060538	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	419	277	93	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	277	277	93	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	277	277	93	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	410	277	93	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	413	277	93	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	410	277	93	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	459	277	93	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658561,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658561,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	533	-	-	-	-	rs876658561,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	415	277	93	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876658561,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658561,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs876658561,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658561,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=973;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658561,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2505;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	416	277	93	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	527	160	54	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	410	160	54	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658561,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658561,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658561,COSV53525400	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=599;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	413	160	54	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	467	160	54	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	410	160	54	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230431	17:7676092-7676092	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	420	160	54	L	Ctg/Ttg	rs876658561,COSV53525400	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	418	276	92	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	276	276	92	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	276	276	92	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	409	276	92	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	412	276	92	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	409	276	92	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	458	276	92	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=600;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=600;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	532	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	414	276	92	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=600;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=974;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2506;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	415	276	92	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	526	159	53	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	409	159	53	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=600;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=600;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=600;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	412	159	53	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	466	159	53	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	409	159	53	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
230925	17:7676093-7676093	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	419	159	53	P	ccC/ccT	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	418	276	92	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	276	276	92	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	276	276	92	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	409	276	92	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	412	276	92	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	409	276	92	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	458	276	92	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=600;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=600;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	532	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	414	276	92	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=600;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=974;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2506;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	415	276	92	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	526	159	53	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	409	159	53	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=600;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=600;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658845,COSV52734896	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=600;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	412	159	53	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	466	159	53	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	409	159	53	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
507597	17:7676093-7676093	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	419	159	53	P	ccC/ccA	rs876658845,COSV52734896	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	412	270	90	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	270	270	90	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	270	270	90	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	403	270	90	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	406	270	90	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	403	270	90	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	452	270	90	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	526	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	408	270	90	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=980;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2512;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	409	270	90	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	520	153	51	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	403	153	51	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	406	153	51	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	460	153	51	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	403	153	51	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1795041	17:7676099-7676099	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	413	153	51	S	tcC/tcG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	412	270	90	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	270	270	90	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	270	270	90	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	403	270	90	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	406	270	90	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	403	270	90	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	452	270	90	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs863224370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs863224370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	526	-	-	-	-	rs863224370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	408	270	90	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs863224370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs863224370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs863224370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs863224370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=980;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs863224370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2512;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	409	270	90	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	520	153	51	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	403	153	51	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs863224370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs863224370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs863224370	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=606;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	406	153	51	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	460	153	51	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	403	153	51	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215761	17:7676099-7676099	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	413	153	51	S	tcC/tcT	rs863224370	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	409	267	89	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	267	267	89	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	267	267	89	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	400	267	89	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	403	267	89	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	400	267	89	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	449	267	89	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	523	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	405	267	89	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=983;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2515;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	406	267	89	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	517	150	50	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	400	150	50	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	403	150	50	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	457	150	50	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	400	150	50	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184403	17:7676102-7676102	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	410	150	50	P	ccC/ccT	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	409	267	89	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	267	267	89	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	267	267	89	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	400	267	89	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	403	267	89	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	400	267	89	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	449	267	89	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	523	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	405	267	89	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=983;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2515;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	406	267	89	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	517	150	50	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	400	150	50	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201443	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=609;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	403	150	50	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	457	150	50	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	400	150	50	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
387623	17:7676102-7676102	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	410	150	50	P	ccC/ccA	rs786201443	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	407	265	89	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	265	265	89	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	265	265	89	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	398	265	89	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	401	265	89	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	398	265	89	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	447	265	89	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374210,COSV52809484	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=611;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374210,COSV52809484	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=611;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	521	-	-	-	-	rs1597374210,COSV52809484	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	403	265	89	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597374210,COSV52809484	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374210,COSV52809484	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=611;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597374210,COSV52809484	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374210,COSV52809484	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=985;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374210,COSV52809484	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2517;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	404	265	89	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	515	148	50	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	398	148	50	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374210,COSV52809484	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=611;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374210,COSV52809484	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=611;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374210,COSV52809484	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=611;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	401	148	50	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	455	148	50	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	398	148	50	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
821636	17:7676104-7676104	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	408	148	50	P/T	Ccc/Acc	rs1597374210,COSV52809484	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	406	264	88	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	264	264	88	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	264	264	88	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	397	264	88	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	400	264	88	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	397	264	88	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	446	264	88	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660951,COSV105024069	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=612;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660951,COSV105024069	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=612;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	520	-	-	-	-	rs876660951,COSV105024069	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	402	264	88	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876660951,COSV105024069	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660951,COSV105024069	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=612;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs876660951,COSV105024069	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660951,COSV105024069	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=986;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660951,COSV105024069	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2518;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	403	264	88	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	514	147	49	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	397	147	49	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660951,COSV105024069	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=612;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660951,COSV105024069	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=612;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876660951,COSV105024069	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=612;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	400	147	49	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	454	147	49	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	397	147	49	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
234239	17:7676105-7676105	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	407	147	49	A	gcC/gcT	rs876660951,COSV105024069	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	403	261	87	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	261	261	87	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	261	261	87	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	394	261	87	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	397	261	87	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	394	261	87	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	443	261	87	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	517	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	399	261	87	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=989;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2521;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	400	261	87	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	511	144	48	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	394	144	48	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	397	144	48	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	451	144	48	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	394	144	48	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1158000	17:7676108-7676108	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	404	144	48	P	ccA/ccT	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	403	261	87	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	261	261	87	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	261	261	87	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	394	261	87	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	397	261	87	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	394	261	87	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	443	261	87	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	517	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	399	261	87	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=989;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2521;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	400	261	87	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	511	144	48	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	394	144	48	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53389010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	397	144	48	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	451	144	48	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	394	144	48	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1674686	17:7676108-7676108	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	404	144	48	P	ccA/ccC	COSV53389010	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	400	258	86	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	258	258	86	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	258	258	86	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	391	258	86	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	394	258	86	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	391	258	86	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	440	258	86	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1445371843,COSV53700583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=618;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1445371843,COSV53700583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=618;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	514	-	-	-	-	rs1445371843,COSV53700583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	396	258	86	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1445371843,COSV53700583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1445371843,COSV53700583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=618;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1445371843,COSV53700583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1445371843,COSV53700583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=992;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1445371843,COSV53700583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2524;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	397	258	86	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	508	141	47	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	391	141	47	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1445371843,COSV53700583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=618;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1445371843,COSV53700583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=618;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1445371843,COSV53700583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=618;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	394	141	47	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	448	141	47	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	391	141	47	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793473	17:7676111-7676111	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	401	141	47	A	gcA/gcG	rs1445371843,COSV53700583	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=0,1;PHENO=0,1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	398	256	86	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	256	256	86	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	256	256	86	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	389	256	86	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	392	256	86	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	389	256	86	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	438	256	86	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	512	-	-	-	-	COSV105877899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	394	256	86	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV105877899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV105877899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=994;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2526;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	395	256	86	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	506	139	47	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	389	139	47	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=620;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	392	139	47	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	446	139	47	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	389	139	47	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1793227	17:7676113-7676113	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	399	139	47	A/P	Gca/Cca	COSV105877899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	397	255	85	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	255	255	85	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	255	255	85	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	388	255	85	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	391	255	85	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	388	255	85	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	437	255	85	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	511	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	393	255	85	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=995;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2527;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	394	255	85	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	505	138	46	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	388	138	46	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	391	138	46	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	445	138	46	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	388	138	46	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
184097	17:7676114-7676114	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	398	138	46	P	ccT/ccC	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	397	255	85	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	255	255	85	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	255	255	85	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	388	255	85	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	391	255	85	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	388	255	85	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	437	255	85	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	511	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	393	255	85	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=995;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2527;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	394	255	85	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	505	138	46	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	388	138	46	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs775515332,COSV105022608	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=621;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	391	138	46	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	445	138	46	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	388	138	46	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186063	17:7676114-7676114	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	398	138	46	P	ccT/ccA	rs775515332,COSV105022608	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	393	251	84	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	251	251	84	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	251	251	84	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	384	251	84	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	387	251	84	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	384	251	84	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	433	251	84	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=625;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=625;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	507	-	-	-	-	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	389	251	84	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=625;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=999;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2531;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	390	251	84	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	501	134	45	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	384	134	45	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=625;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=625;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=625;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	387	134	45	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	441	134	45	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	384	134	45	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
1792511	17:7676118-7676118	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	394	134	45	A/V	gCc/gTc	COSV52751073,COSV52850626,COSV53292497	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1,1;PHENO=1,1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	392	250	84	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	250	250	84	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	250	250	84	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	383	250	84	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	386	250	84	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	383	250	84	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	432	250	84	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781307,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781307,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	506	-	-	-	-	rs587781307,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	388	250	84	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587781307,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781307,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587781307,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781307,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1000;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781307,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2532;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	389	250	84	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	500	133	45	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	383	133	45	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781307,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781307,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781307,COSV53077353	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=626;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	386	133	45	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	440	133	45	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	383	133	45	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
140833	17:7676119-7676119	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	393	133	45	A/T	Gcc/Acc	rs587781307,COSV53077353	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	391	249	83	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	249	249	83	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	249	249	83	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	382	249	83	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	385	249	83	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	382	249	83	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	431	249	83	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs55754907,COSV52916975	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs55754907,COSV52916975	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	505	-	-	-	-	rs55754907,COSV52916975	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	387	249	83	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs55754907,COSV52916975	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs55754907,COSV52916975	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs55754907,COSV52916975	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs55754907,COSV52916975	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1001;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs55754907,COSV52916975	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2533;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	388	249	83	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	499	132	44	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	382	132	44	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs55754907,COSV52916975	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs55754907,COSV52916975	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs55754907,COSV52916975	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=627;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	385	132	44	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	439	132	44	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	382	132	44	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
186003	17:7676120-7676120	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	392	132	44	A	gcG/gcA	rs55754907,COSV52916975	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	388	246	82	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	246	246	82	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	246	246	82	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	379	246	82	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	382	246	82	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	379	246	82	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	428	246	82	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	502	-	-	-	-	COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	384	246	82	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1004;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2536;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	385	246	82	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	496	129	43	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	379	129	43	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	382	129	43	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	436	129	43	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	379	129	43	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1791760	17:7676123-7676123	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	389	129	43	P	ccG/ccC	COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	388	246	82	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	246	246	82	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	246	246	82	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	379	246	82	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	382	246	82	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	379	246	82	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	428	246	82	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs372397095,COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs372397095,COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	502	-	-	-	-	rs372397095,COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	384	246	82	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs372397095,COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs372397095,COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs372397095,COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs372397095,COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1004;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs372397095,COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2536;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	385	246	82	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	496	129	43	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	379	129	43	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs372397095,COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs372397095,COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs372397095,COSV52772507,COSV52972073	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=630;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	382	129	43	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	436	129	43	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	379	129	43	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184721	17:7676123-7676123	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	389	129	43	P	ccG/ccA	rs372397095,COSV52772507,COSV52972073	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,benign/likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	385	243	81	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	243	243	81	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	243	243	81	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	376	243	81	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	379	243	81	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	376	243	81	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	425	243	81	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	499	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	381	243	81	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1007;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2539;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	382	243	81	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	493	126	42	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	376	126	42	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	379	126	42	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	433	126	42	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	376	126	42	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1791285	17:7676126-7676126	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	386	126	42	T	acA/acT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	385	243	81	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	243	243	81	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	243	243	81	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	376	243	81	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	379	243	81	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	376	243	81	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	425	243	81	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	499	-	-	-	-	rs1597374412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	381	243	81	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597374412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597374412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1007;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2539;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	382	243	81	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	493	126	42	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	376	126	42	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374412	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=633;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	379	126	42	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	433	126	42	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	376	126	42	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793102	17:7676126-7676126	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	386	126	42	T	acA/acG	rs1597374412	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	379	237	79	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	237	237	79	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	237	237	79	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	370	237	79	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	373	237	79	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	370	237	79	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	419	237	79	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	493	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	375	237	79	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1013;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2545;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	376	237	79	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	487	120	40	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	370	120	40	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	373	120	40	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	427	120	40	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	370	120	40	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1171926	17:7676132-7676132	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	380	120	40	A	gcT/gcG	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	379	237	79	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	237	237	79	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	237	237	79	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	370	237	79	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	373	237	79	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	370	237	79	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	419	237	79	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	493	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	375	237	79	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1013;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2545;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	376	237	79	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	487	120	40	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	370	120	40	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53704482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=639;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	373	120	40	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	427	120	40	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	370	120	40	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1790426	17:7676132-7676132	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	380	120	40	A	gcT/gcC	COSV53704482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	376	234	78	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	234	234	78	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	234	234	78	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	367	234	78	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	370	234	78	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	367	234	78	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	416	234	78	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs375099397	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=642;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs375099397	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=642;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	490	-	-	-	-	rs375099397	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	372	234	78	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs375099397	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs375099397	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=642;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs375099397	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs375099397	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1016;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs375099397	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2548;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	373	234	78	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	484	117	39	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	367	117	39	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs375099397	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=642;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs375099397	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=642;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs375099397	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=642;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	370	117	39	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	424	117	39	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	367	117	39	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
183835	17:7676135-7676135	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	377	117	39	A	gcA/gcG	rs375099397	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	370	228	76	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	228	228	76	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	228	228	76	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	361	228	76	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	364	228	76	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	361	228	76	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	410	228	76	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52760638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52760638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	484	-	-	-	-	COSV52760638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	366	228	76	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52760638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52760638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52760638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52760638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1022;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52760638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2554;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	367	228	76	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	478	111	37	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	361	111	37	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52760638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52760638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52760638	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=648;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	364	111	37	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	418	111	37	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	361	111	37	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789064	17:7676141-7676141	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	371	111	37	A	gcA/gcG	COSV52760638	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	364	222	74	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	222	222	74	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	222	222	74	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	355	222	74	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	358	222	74	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	355	222	74	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	404	222	74	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201577,COSV52994858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=654;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201577,COSV52994858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=654;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	478	-	-	-	-	rs786201577,COSV52994858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	360	222	74	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs786201577,COSV52994858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201577,COSV52994858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=654;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs786201577,COSV52994858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201577,COSV52994858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1028;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201577,COSV52994858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2560;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	361	222	74	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	472	105	35	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	355	105	35	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201577,COSV52994858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=654;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201577,COSV52994858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=654;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201577,COSV52994858	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=654;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	358	105	35	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	412	105	35	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	355	105	35	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
184625	17:7676147-7676147	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	365	105	35	A	gcC/gcT	rs786201577,COSV52994858	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	363	221	74	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	221	221	74	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	221	221	74	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	354	221	74	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	357	221	74	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	354	221	74	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	403	221	74	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781832,COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781832,COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	477	-	-	-	-	rs587781832,COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	359	221	74	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587781832,COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781832,COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587781832,COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781832,COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1029;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781832,COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2561;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	360	221	74	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	471	104	35	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	354	104	35	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781832,COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781832,COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781832,COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	357	104	35	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	411	104	35	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	354	104	35	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
141547	17:7676148-7676148	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	364	104	35	A/V	gCc/gTc	rs587781832,COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1,1;PHENO=1,1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	363	221	74	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	221	221	74	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	221	221	74	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	354	221	74	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	357	221	74	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	354	221	74	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	403	221	74	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	477	-	-	-	-	COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	359	221	74	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1029;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2561;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	360	221	74	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	471	104	35	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	354	104	35	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52671187,COSV53086204	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=655;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	357	104	35	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	411	104	35	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	354	104	35	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1787901	17:7676148-7676148	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	364	104	35	A/G	gCc/gGc	COSV52671187,COSV53086204	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	361	219	73	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	219	219	73	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	219	219	73	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	352	219	73	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	355	219	73	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	352	219	73	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	401	219	73	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52851457	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=657;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52851457	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=657;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	475	-	-	-	-	COSV52851457	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	357	219	73	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52851457	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52851457	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=657;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52851457	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52851457	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1031;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52851457	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2563;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	358	219	73	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	469	102	34	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	352	102	34	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52851457	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=657;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52851457	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=657;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52851457	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=657;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	355	102	34	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	409	102	34	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	352	102	34	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
918263	17:7676150-7676150	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	362	102	34	V	gtG/gtT	COSV52851457	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	358	216	72	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	216	216	72	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	216	216	72	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	349	216	72	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	352	216	72	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	349	216	72	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	398	216	72	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs56275308,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs56275308,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	472	-	-	-	-	rs56275308,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	354	216	72	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs56275308,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs56275308,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs56275308,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs56275308,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1034;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs56275308,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2566;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	355	216	72	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	466	99	33	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	349	99	33	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs56275308,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs56275308,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs56275308,COSV104586728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	352	99	33	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	406	99	33	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	349	99	33	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
184372	17:7676153-7676153	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	359	99	33	P	ccC/ccT	rs56275308,COSV104586728	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;SOMATIC=0,1;PHENO=1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	357-358	215-216	72	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	215-216	215-216	72	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	215-216	215-216	72	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	348-349	215-216	72	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	351-352	215-216	72	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	348-349	215-216	72	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	397-398	215-216	72	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854066,COSV52847066,COSV99452237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854066,COSV52847066,COSV99452237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	471-472	-	-	-	-	rs878854066,COSV52847066,COSV99452237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	353-354	215-216	72	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs878854066,COSV52847066,COSV99452237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854066,COSV52847066,COSV99452237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs878854066,COSV52847066,COSV99452237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854066,COSV52847066,COSV99452237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1034;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854066,COSV52847066,COSV99452237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2566;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	354-355	215-216	72	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	465-466	98-99	33	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	348-349	98-99	33	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854066,COSV52847066,COSV99452237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854066,COSV52847066,COSV99452237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854066,COSV52847066,COSV99452237	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=660;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	351-352	98-99	33	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	405-406	98-99	33	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	348-349	98-99	33	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
237944	17:7676153-7676154	AC	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	358-359	98-99	33	P/R	cCC/cGT	rs878854066,COSV52847066,COSV99452237	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	355	213	71	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	213	213	71	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	213	213	71	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	346	213	71	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	349	213	71	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	346	213	71	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	395	213	71	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526701,COSV99431187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=663;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526701,COSV99431187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=663;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	469	-	-	-	-	rs1555526701,COSV99431187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	351	213	71	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526701,COSV99431187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526701,COSV99431187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=663;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526701,COSV99431187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526701,COSV99431187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1037;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526701,COSV99431187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2569;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	352	213	71	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	463	96	32	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	346	96	32	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526701,COSV99431187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=663;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526701,COSV99431187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=663;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526701,COSV99431187	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=663;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	349	96	32	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	403	96	32	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	346	96	32	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
514039	17:7676156-7676156	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	356	96	32	P	ccC/ccT	rs1555526701,COSV99431187	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	352	210	70	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	210	210	70	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	210	210	70	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	343	210	70	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	346	210	70	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	343	210	70	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	392	210	70	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	466	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	348	210	70	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1040;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2572;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	349	210	70	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	460	93	31	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	343	93	31	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	346	93	31	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	400	93	31	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	343	93	31	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187153	17:7676159-7676159	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	353	93	31	A	gcT/gcC	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	352	210	70	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	210	210	70	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	210	210	70	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	343	210	70	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	346	210	70	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	343	210	70	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	392	210	70	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	466	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	348	210	70	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1040;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2572;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	349	210	70	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	460	93	31	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	343	93	31	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203513,COSV53016917	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=666;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	346	93	31	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	400	93	31	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	343	93	31	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414038	17:7676159-7676159	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	353	93	31	A	gcT/gcA	rs786203513,COSV53016917	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	349	207	69	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	207	207	69	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	207	207	69	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	340	207	69	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	343	207	69	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	340	207	69	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	389	207	69	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs775185978,COSV52742379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=669;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs775185978,COSV52742379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=669;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	463	-	-	-	-	rs775185978,COSV52742379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	345	207	69	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs775185978,COSV52742379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs775185978,COSV52742379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=669;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs775185978,COSV52742379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs775185978,COSV52742379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1043;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs775185978,COSV52742379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2575;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	346	207	69	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	457	90	30	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	340	90	30	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs775185978,COSV52742379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=669;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs775185978,COSV52742379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=669;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs775185978,COSV52742379	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=669;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	343	90	30	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	397	90	30	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	340	90	30	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
219841	17:7676162-7676162	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	350	90	30	A	gcT/gcC	rs775185978,COSV52742379	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	346	204	68	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	204	204	68	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	204	204	68	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	337	204	68	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	340	204	68	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	337	204	68	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	386	204	68	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs746814615,COSV106055898,COSV53163150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=672;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs746814615,COSV106055898,COSV53163150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=672;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	460	-	-	-	-	rs746814615,COSV106055898,COSV53163150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	342	204	68	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs746814615,COSV106055898,COSV53163150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs746814615,COSV106055898,COSV53163150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=672;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs746814615,COSV106055898,COSV53163150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs746814615,COSV106055898,COSV53163150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1046;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs746814615,COSV106055898,COSV53163150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2578;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	343	204	68	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	454	87	29	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	337	87	29	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs746814615,COSV106055898,COSV53163150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=672;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs746814615,COSV106055898,COSV53163150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=672;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs746814615,COSV106055898,COSV53163150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=672;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	340	87	29	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	394	87	29	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	337	87	29	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
185003	17:7676165-7676165	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	347	87	29	E	gaG/gaA	rs746814615,COSV106055898,COSV53163150	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	343	201	67	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	201	201	67	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	201	201	67	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	334	201	67	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	337	201	67	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	334	201	67	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	383	201	67	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203912,COSV53527515,COSV53883057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=675;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203912,COSV53527515,COSV53883057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=675;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	457	-	-	-	-	rs786203912,COSV53527515,COSV53883057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	339	201	67	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs786203912,COSV53527515,COSV53883057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203912,COSV53527515,COSV53883057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=675;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs786203912,COSV53527515,COSV53883057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203912,COSV53527515,COSV53883057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1049;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203912,COSV53527515,COSV53883057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2581;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	340	201	67	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	451	84	28	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	334	84	28	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203912,COSV53527515,COSV53883057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=675;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203912,COSV53527515,COSV53883057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=675;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786203912,COSV53527515,COSV53883057	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=675;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	337	84	28	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	391	84	28	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	334	84	28	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
187675	17:7676168-7676168	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	344	84	28	P	ccA/ccG	rs786203912,COSV53527515,COSV53883057	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	338	196	66	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	196	196	66	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	196	196	66	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	329	196	66	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	332	196	66	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	329	196	66	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	378	196	66	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=680;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=680;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	452	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	334	196	66	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=680;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1054;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2586;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	335	196	66	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	446	79	27	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	329	79	27	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=680;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=680;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=680;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	332	79	27	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	386	79	27	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	329	79	27	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1783578	17:7676173-7676173	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	339	79	27	M/V	Atg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	337	195	65	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	195	195	65	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	195	195	65	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	328	195	65	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	331	195	65	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	328	195	65	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	377	195	65	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=681;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=681;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	451	-	-	-	-	rs1597374742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	333	195	65	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597374742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=681;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597374742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1055;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2587;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	334	195	65	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	445	78	26	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	328	78	26	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=681;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=681;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374742	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=681;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	331	78	26	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	385	78	26	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	328	78	26	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
793034	17:7676174-7676174	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	338	78	26	R	agA/agG	rs1597374742	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	335	193	65	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	193	193	65	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	193	193	65	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	326	193	65	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	329	193	65	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	326	193	65	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	375	193	65	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	449	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	331	193	65	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2589;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	332	193	65	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	443	76	26	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	326	76	26	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526721,COSV52689560	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=683;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	329	76	26	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	383	76	26	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	326	76	26	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
485031	17:7676176-7676176	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	336	76	26	R	Aga/Cga	rs1555526721,COSV52689560	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	334	192	64	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	192	192	64	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	192	192	64	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	325	192	64	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	328	192	64	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	325	192	64	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	374	192	64	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526723,CD065798	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=684;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526723,CD065798	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=684;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	448	-	-	-	-	rs1555526723,CD065798	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	330	192	64	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526723,CD065798	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526723,CD065798	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=684;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526723,CD065798	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526723,CD065798	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1058;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526723,CD065798	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2590;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	331	192	64	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	442	75	25	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	325	75	25	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526723,CD065798	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=684;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526723,CD065798	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=684;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526723,CD065798	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=684;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	328	75	25	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	382	75	25	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	325	75	25	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
458526	17:7676177-7676177	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	335	75	25	P	ccC/ccG	rs1555526723,CD065798	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	331	189	63	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	189	189	63	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	189	189	63	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	322	189	63	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	325	189	63	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	322	189	63	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	371	189	63	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	CX114002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=687;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	CX114002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=687;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	445	-	-	-	-	CX114002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	327	189	63	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	CX114002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	CX114002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=687;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	CX114002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CX114002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1061;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CX114002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2593;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	328	189	63	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	439	72	24	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	322	72	24	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	CX114002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=687;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	CX114002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=687;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	CX114002	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=687;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	325	72	24	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	379	72	24	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	322	72	24	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1086600	17:7676180-7676180	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	332	72	24	A	gcT/gcC	CX114002	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	330	188	63	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	188	188	63	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	188	188	63	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	321	188	63	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	324	188	63	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	321	188	63	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	370	188	63	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	444	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	326	188	63	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1062;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2594;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	327	188	63	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	438	71	24	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	321	71	24	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs372201428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=688;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	324	71	24	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	378	71	24	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	321	71	24	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
229693	17:7676181-7676181	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	331	71	24	A/G	gCt/gGt	rs372201428	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;PHENO=1
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	325	183	61	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	183	183	61	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	183	183	61	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	316	183	61	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	319	183	61	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	316	183	61	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	365	183	61	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=693;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=693;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	439	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	321	183	61	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=693;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1067;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2599;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	322	183	61	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	433	66	22	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	316	66	22	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=693;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=693;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=693;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	319	66	22	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	373	66	22	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	316	66	22	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1329426	17:7676186-7676186	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	326	66	22	D	gaT/gaC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	322	180	60	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	180	180	60	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	180	180	60	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	313	180	60	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	316	180	60	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	313	180	60	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	362	180	60	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	436	-	-	-	-	COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	318	180	60	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1070;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2602;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	319	180	60	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	430	63	21	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	313	63	21	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	316	63	21	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	370	63	21	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	313	63	21	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1780538	17:7676189-7676189	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	323	63	21	P	ccA/ccG	COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	322	180	60	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	180	180	60	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	180	180	60	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	313	180	60	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	316	180	60	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	313	180	60	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	362	180	60	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs749289195,COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs749289195,COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	436	-	-	-	-	rs749289195,COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	318	180	60	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs749289195,COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs749289195,COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs749289195,COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs749289195,COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1070;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs749289195,COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2602;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	319	180	60	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	430	63	21	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	313	63	21	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs749289195,COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs749289195,COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs749289195,COSV53097091	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=696;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	316	63	21	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	370	63	21	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	313	63	21	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
185834	17:7676189-7676189	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	323	63	21	P	ccA/ccC	rs749289195,COSV53097091	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	319	177	59	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	177	177	59	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	177	177	59	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	310	177	59	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	313	177	59	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	310	177	59	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	359	177	59	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=699;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=699;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	433	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	315	177	59	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=699;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1073;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2605;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	316	177	59	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	427	60	20	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	310	60	20	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=699;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=699;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=699;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	313	60	20	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	367	60	20	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	310	60	20	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1779968	17:7676192-7676192	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	320	60	20	G	ggT/ggA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	318	176	59	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	176	176	59	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	176	176	59	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	309	176	59	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	312	176	59	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	309	176	59	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	358	176	59	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374828,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=700;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374828,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=700;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	432	-	-	-	-	rs1597374828,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	314	176	59	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597374828,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374828,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=700;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597374828,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374828,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374828,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2606;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	315	176	59	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	426	59	20	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	309	59	20	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374828,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=700;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374828,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=700;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597374828,COSV53624897	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=700;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	312	59	20	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	366	59	20	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	309	59	20	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
820048	17:7676193-7676193	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	319	59	20	G/D	gGt/gAt	rs1597374828,COSV53624897	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	316	174	58	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	174	174	58	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	174	174	58	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	307	174	58	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	310	174	58	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	307	174	58	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	356	174	58	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504166,COSV52983469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=702;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504166,COSV52983469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=702;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	430	-	-	-	-	rs1060504166,COSV52983469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	312	174	58	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1060504166,COSV52983469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504166,COSV52983469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=702;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1060504166,COSV52983469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504166,COSV52983469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1076;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504166,COSV52983469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2608;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	313	174	58	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	424	57	19	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	307	57	19	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504166,COSV52983469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=702;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504166,COSV52983469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=702;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504166,COSV52983469	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=702;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	310	57	19	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	364	57	19	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	307	57	19	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414034	17:7676195-7676195	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	317	57	19	P	ccA/ccG	rs1060504166,COSV52983469	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	314	172	58	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	172	172	58	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	172	172	58	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	305	172	58	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	308	172	58	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	305	172	58	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	354	172	58	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586115	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=704;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586115	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=704;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	428	-	-	-	-	COSV104586115	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	310	172	58	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV104586115	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586115	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=704;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV104586115	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586115	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1078;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586115	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2610;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	311	172	58	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	422	55	19	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	305	55	19	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586115	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=704;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586115	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=704;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV104586115	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=704;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	308	55	19	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	362	55	19	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	305	55	19	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778944	17:7676197-7676197	C	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	315	55	19	P/A	Cca/Gca	COSV104586115	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	313	171	57	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	171	171	57	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	171	171	57	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	304	171	57	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	307	171	57	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	304	171	57	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	353	171	57	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782776,COSV52774842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=705;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782776,COSV52774842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=705;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	427	-	-	-	-	rs587782776,COSV52774842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	309	171	57	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587782776,COSV52774842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782776,COSV52774842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=705;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587782776,COSV52774842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782776,COSV52774842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1079;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782776,COSV52774842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2611;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	310	171	57	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	421	54	18	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	304	54	18	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782776,COSV52774842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=705;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782776,COSV52774842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=705;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587782776,COSV52774842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=705;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	307	54	18	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	361	54	18	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	304	54	18	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
486558	17:7676198-7676198	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	314	54	18	D	gaC/gaT	rs587782776,COSV52774842	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	312	170	57	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	170	170	57	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	170	170	57	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	303	170	57	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	306	170	57	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	303	170	57	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	352	170	57	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=706;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=706;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	426	-	-	-	-	COSV105877948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	308	170	57	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV105877948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=706;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV105877948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1080;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2612;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	309	170	57	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	420	53	18	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	303	53	18	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=706;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=706;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV105877948	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=706;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	306	53	18	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	360	53	18	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	303	53	18	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1778520	17:7676199-7676199	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	313	53	18	D/V	gAc/gTc	COSV105877948	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	310	168	56	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	168	168	56	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	168	168	56	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	301	168	56	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	304	168	56	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	301	168	56	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	350	168	56	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs574255227,COSV53067968	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=708;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs574255227,COSV53067968	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=708;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	424	-	-	-	-	rs574255227,COSV53067968	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	306	168	56	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs574255227,COSV53067968	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs574255227,COSV53067968	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=708;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs574255227,COSV53067968	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs574255227,COSV53067968	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1082;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs574255227,COSV53067968	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2614;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	307	168	56	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	418	51	17	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	301	51	17	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs574255227,COSV53067968	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=708;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs574255227,COSV53067968	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=708;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs574255227,COSV53067968	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=708;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	304	51	17	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	358	51	17	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	301	51	17	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215760	17:7676201-7676201	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	311	51	17	E	gaA/gaG	rs574255227,COSV53067968	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	307	165	55	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	165	165	55	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	165	165	55	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	298	165	55	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	301	165	55	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	298	165	55	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	347	165	55	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53293945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=711;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53293945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=711;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	421	-	-	-	-	COSV53293945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	303	165	55	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53293945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53293945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=711;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV53293945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53293945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1085;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53293945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2617;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	304	165	55	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	415	48	16	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	298	48	16	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53293945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=711;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53293945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=711;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53293945	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=711;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	301	48	16	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	355	48	16	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	298	48	16	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1126030	17:7676204-7676204	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	308	48	16	T	acT/acG	COSV53293945	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	302	160	54	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	160	160	54	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	160	160	54	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	293	160	54	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	296	160	54	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	293	160	54	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	342	160	54	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=716;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=716;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	416	-	-	-	-	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	298	160	54	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=716;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2622;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	299	160	54	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	410	43	15	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	293	43	15	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=716;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=716;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=716;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	296	43	15	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	350	43	15	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	293	43	15	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
481098	17:7676209-7676209	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	303	43	15	F/L	Ttc/Ctc	rs1555526742,COSV52729490,COSV53731884	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	300	158	53	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	158	158	53	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	158	158	53	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	291	158	53	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	294	158	53	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	291	158	53	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	340	158	53	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	414	-	-	-	-	COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	296	158	53	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1092;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2624;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	297	158	53	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	408	41	14	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	291	41	14	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52774899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=718;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	294	41	14	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	348	41	14	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	291	41	14	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1775891	17:7676211-7676211	A	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	301	41	14	W/L	tGg/tTg	COSV52774899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	298	156	52	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	156	156	52	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	156	156	52	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	289	156	52	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	292	156	52	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	289	156	52	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	338	156	52	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523702,COSV53380575,COSV53638110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523702,COSV53380575,COSV53638110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	412	-	-	-	-	rs1057523702,COSV53380575,COSV53638110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	294	156	52	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1057523702,COSV53380575,COSV53638110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523702,COSV53380575,COSV53638110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1057523702,COSV53380575,COSV53638110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523702,COSV53380575,COSV53638110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1094;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523702,COSV53380575,COSV53638110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2626;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	295	156	52	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	406	39	13	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	289	39	13	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523702,COSV53380575,COSV53638110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523702,COSV53380575,COSV53638110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057523702,COSV53380575,COSV53638110	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=720;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	292	39	13	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	346	39	13	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	289	39	13	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
390266	17:7676213-7676213	C	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	299	39	13	Q	caA/caG	rs1057523702,COSV53380575,COSV53638110	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	291	149	50	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	149	149	50	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	149	149	50	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	282	149	50	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	285	149	50	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	282	149	50	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	331	149	50	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs370502517,COSV52758078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=727;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs370502517,COSV52758078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=727;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	405	-	-	-	-	rs370502517,COSV52758078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	287	149	50	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs370502517,COSV52758078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs370502517,COSV52758078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=727;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs370502517,COSV52758078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs370502517,COSV52758078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1101;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs370502517,COSV52758078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2633;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	288	149	50	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	399	32	11	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	282	32	11	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs370502517,COSV52758078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=727;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs370502517,COSV52758078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=727;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs370502517,COSV52758078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=727;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	285	32	11	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	339	32	11	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	282	32	11	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
216464	17:7676220-7676220	G	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	292	32	11	I/T	aTt/aCt	rs370502517,COSV52758078	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	289	147	49	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	147	147	49	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	147	147	49	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	280	147	49	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	283	147	49	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	280	147	49	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	329	147	49	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=729;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=729;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	403	-	-	-	-	rs786201148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	285	147	49	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs786201148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=729;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs786201148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1103;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2635;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	286	147	49	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	397	30	10	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	280	30	10	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=729;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=729;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=729;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	283	30	10	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	337	30	10	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	280	30	10	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183901	17:7676222-7676222	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	290	30	10	D	gaT/gaC	rs786201148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	286	144	48	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	144	144	48	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	144	144	48	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	277	144	48	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	280	144	48	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	277	144	48	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	326	144	48	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=732;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=732;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	400	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	282	144	48	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=732;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1106;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2638;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	283	144	48	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000610292.4	Transcript	missense_variant	394	27	9	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000610538.4	Transcript	missense_variant	277	27	9	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=732;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=732;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=732;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000619485.4	Transcript	missense_variant	280	27	9	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000620739.4	Transcript	missense_variant	334	27	9	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000622645.4	Transcript	missense_variant	277	27	9	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
141056	17:7676225-7676225	T	ENSG00000141510	ENST00000635293.1	Transcript	missense_variant,NMD_transcript_variant	287	27	9	D/E	gaC/gaA	rs587781460,COSV53152246,COSV53510615	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	286	144	48	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	144	144	48	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	144	144	48	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	277	144	48	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	280	144	48	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	277	144	48	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	326	144	48	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=732;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=732;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	400	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	282	144	48	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=732;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1106;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2638;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	283	144	48	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	394	27	9	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	277	27	9	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=732;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=732;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781460,COSV53152246,COSV53510615	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=732;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	280	27	9	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	334	27	9	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	277	27	9	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
233189	17:7676225-7676225	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	287	27	9	D	gaC/gaT	rs587781460,COSV53152246,COSV53510615	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	283	141	47	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	141	141	47	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	141	141	47	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	274	141	47	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	277	141	47	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	274	141	47	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	323	141	47	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	397	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	279	141	47	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1109;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2641;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	280	141	47	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	391	24	8	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	274	24	8	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	277	24	8	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	331	24	8	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	274	24	8	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1096501	17:7676228-7676228	A	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	284	24	8	P	ccG/ccT	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	283	141	47	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	141	141	47	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	141	141	47	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	274	141	47	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	277	141	47	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	274	141	47	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	323	141	47	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	397	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	279	141	47	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1109;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2641;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	280	141	47	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	391	24	8	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	274	24	8	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs201741778,COSV53169768,COSV53225368	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=735;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	277	24	8	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	331	24	8	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	274	24	8	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
184839	17:7676228-7676228	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	284	24	8	P	ccG/ccA	rs201741778,COSV53169768,COSV53225368	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	277	135	45	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	135	135	45	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	135	135	45	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	268	135	45	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	271	135	45	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	268	135	45	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	317	135	45	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504164,COSV53280631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=741;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504164,COSV53280631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=741;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	391	-	-	-	-	rs1060504164,COSV53280631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	273	135	45	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1060504164,COSV53280631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504164,COSV53280631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=741;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1060504164,COSV53280631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504164,COSV53280631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1115;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504164,COSV53280631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2647;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	274	135	45	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	385	18	6	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	268	18	6	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504164,COSV53280631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=741;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504164,COSV53280631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=741;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1060504164,COSV53280631	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=741;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	271	18	6	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	325	18	6	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	268	18	6	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414031	17:7676234-7676234	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	278	18	6	L	ctG/ctA	rs1060504164,COSV53280631	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	271	129	43	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	129	129	43	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	129	129	43	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	262	129	43	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	265	129	43	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	262	129	43	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	311	129	43	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52670301,COSV53353969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52670301,COSV53353969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	385	-	-	-	-	COSV52670301,COSV53353969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	267	129	43	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52670301,COSV53353969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52670301,COSV53353969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52670301,COSV53353969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52670301,COSV53353969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1121;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52670301,COSV53353969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2653;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	268	129	43	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	379	12	4	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	262	12	4	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52670301,COSV53353969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52670301,COSV53353969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52670301,COSV53353969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=747;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	265	12	4	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	319	12	4	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	262	12	4	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1151675	17:7676240-7676240	T	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	272	12	4	L	ttG/ttA	COSV52670301,COSV53353969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	269	127	43	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	127	127	43	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	127	127	43	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	260	127	43	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	263	127	43	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	260	127	43	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	309	127	43	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=749;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=749;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	383	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	265	127	43	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=749;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1123;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2655;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	266	127	43	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	377	10	4	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	260	10	4	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=749;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=749;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=749;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	263	10	4	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	317	10	4	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	260	10	4	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767687	17:7676242-7676242	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	270	10	4	L	Ttg/Ctg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	268	126	42	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	126	126	42	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	126	126	42	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	259	126	42	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	262	126	42	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	259	126	42	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	308	126	42	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375122,COSV52674208,COSV53415078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=750;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375122,COSV52674208,COSV53415078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=750;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	382	-	-	-	-	rs1597375122,COSV52674208,COSV53415078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	264	126	42	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597375122,COSV52674208,COSV53415078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375122,COSV52674208,COSV53415078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=750;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597375122,COSV52674208,COSV53415078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375122,COSV52674208,COSV53415078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1124;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375122,COSV52674208,COSV53415078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2656;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	265	126	42	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	376	9	3	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	259	9	3	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375122,COSV52674208,COSV53415078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=750;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375122,COSV52674208,COSV53415078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=750;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375122,COSV52674208,COSV53415078	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=750;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	262	9	3	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	316	9	3	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	259	9	3	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
719297	17:7676243-7676243	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	269	9	3	D	gaT/gaC	rs1597375122,COSV52674208,COSV53415078	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	265	123	41	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	123	123	41	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	123	123	41	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	256	123	41	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	259	123	41	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	256	123	41	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	305	123	41	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs369129220	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=753;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs369129220	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=753;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	379	-	-	-	-	rs369129220	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	261	123	41	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs369129220	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs369129220	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=753;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs369129220	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs369129220	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1127;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs369129220	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2659;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	262	123	41	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000610292.4	Transcript	synonymous_variant	373	6	2	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000610538.4	Transcript	synonymous_variant	256	6	2	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs369129220	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=753;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs369129220	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=753;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs369129220	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=753;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000619485.4	Transcript	synonymous_variant	259	6	2	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000620739.4	Transcript	synonymous_variant	313	6	2	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000622645.4	Transcript	synonymous_variant	256	6	2	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
183721	17:7676246-7676246	G	ENSG00000141510	ENST00000635293.1	Transcript	synonymous_variant,NMD_transcript_variant	266	6	2	D	gaT/gaC	rs369129220	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	259	117	39	A	gcA/gcG	rs1597375167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	117	117	39	A	gcA/gcG	rs1597375167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	117	117	39	A	gcA/gcG	rs1597375167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	250	117	39	A	gcA/gcG	rs1597375167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	253	117	39	A	gcA/gcG	rs1597375167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	250	117	39	A	gcA/gcG	rs1597375167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	299	117	39	A	gcA/gcG	rs1597375167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	373	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	255	117	39	A	gcA/gcG	rs1597375167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1133;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2665;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	256	117	39	A	gcA/gcG	rs1597375167	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	367	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	250	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=759;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	253	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	307	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	250	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
794159	17:7676252-7676252	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	260	-	-	-	-	rs1597375167	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	253	111	37	S	tcC/tcT	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	111	111	37	S	tcC/tcT	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	111	111	37	S	tcC/tcT	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	244	111	37	S	tcC/tcT	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	247	111	37	S	tcC/tcT	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	244	111	37	S	tcC/tcT	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	293	111	37	S	tcC/tcT	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=765;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=765;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	367	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	249	111	37	S	tcC/tcT	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=765;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1139;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2671;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	250	111	37	S	tcC/tcT	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	361	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	244	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=765;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=765;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=765;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	247	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	301	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	244	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458518	17:7676258-7676258	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	254	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	253	111	37	S	tcC/tcG	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	111	111	37	S	tcC/tcG	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	111	111	37	S	tcC/tcG	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	244	111	37	S	tcC/tcG	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	247	111	37	S	tcC/tcG	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	244	111	37	S	tcC/tcG	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	293	111	37	S	tcC/tcG	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=765;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=765;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	367	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	249	111	37	S	tcC/tcG	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=765;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1139;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2671;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	250	111	37	S	tcC/tcG	rs1555526798,COSV105016535	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	361	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	244	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=765;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=765;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=765;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	247	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	301	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	244	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492572	17:7676258-7676258	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	254	-	-	-	-	rs1555526798,COSV105016535	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	250	108	36	P	ccG/ccA	rs1800370,COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	108	108	36	P	ccG/ccA	rs1800370,COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	108	108	36	P	ccG/ccA	rs1800370,COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	241	108	36	P	ccG/ccA	rs1800370,COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	244	108	36	P	ccG/ccA	rs1800370,COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	241	108	36	P	ccG/ccA	rs1800370,COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	290	108	36	P	ccG/ccA	rs1800370,COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=768;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=768;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	364	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	246	108	36	P	ccG/ccA	rs1800370,COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=768;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1142;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2674;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	247	108	36	P	ccG/ccA	rs1800370,COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	358	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	241	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=768;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=768;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=768;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	244	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	298	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	241	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
132708	17:7676261-7676261	T	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	251	-	-	-	-	rs1800370,COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	250	108	36	P	ccG/ccT	COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	108	108	36	P	ccG/ccT	COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	108	108	36	P	ccG/ccT	COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	241	108	36	P	ccG/ccT	COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	244	108	36	P	ccG/ccT	COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	241	108	36	P	ccG/ccT	COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	290	108	36	P	ccG/ccT	COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=768;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=768;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	364	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	246	108	36	P	ccG/ccT	COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=768;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1142;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2674;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	247	108	36	P	ccG/ccT	COSV52756428	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	358	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	241	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=768;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=768;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=768;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	244	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	298	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	241	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1789002	17:7676261-7676261	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	251	-	-	-	-	COSV52756428	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	249	107	36	P/Q	cCg/cAg	rs587781866,COSV53085732	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	107	107	36	P/Q	cCg/cAg	rs587781866,COSV53085732	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	107	107	36	P/Q	cCg/cAg	rs587781866,COSV53085732	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	240	107	36	P/Q	cCg/cAg	rs587781866,COSV53085732	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	243	107	36	P/Q	cCg/cAg	rs587781866,COSV53085732	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	240	107	36	P/Q	cCg/cAg	rs587781866,COSV53085732	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	289	107	36	P/Q	cCg/cAg	rs587781866,COSV53085732	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=769;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=769;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	363	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	245	107	36	P/Q	cCg/cAg	rs587781866,COSV53085732	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=769;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1143;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2675;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	246	107	36	P/Q	cCg/cAg	rs587781866,COSV53085732	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	357	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	240	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=769;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=769;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=769;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	243	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	297	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	240	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
141597	17:7676262-7676262	T	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	250	-	-	-	-	rs587781866,COSV53085732	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	244	102	34	P	ccC/ccG	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	102	102	34	P	ccC/ccG	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	102	102	34	P	ccC/ccG	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	235	102	34	P	ccC/ccG	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	238	102	34	P	ccC/ccG	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	235	102	34	P	ccC/ccG	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	284	102	34	P	ccC/ccG	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	358	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	240	102	34	P	ccC/ccG	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1148;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2680;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	241	102	34	P	ccC/ccG	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	352	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	235	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	238	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	292	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	235	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
186290	17:7676267-7676267	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	245	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	244	102	34	P	ccC/ccT	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	102	102	34	P	ccC/ccT	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	102	102	34	P	ccC/ccT	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	235	102	34	P	ccC/ccT	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	238	102	34	P	ccC/ccT	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	235	102	34	P	ccC/ccT	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	284	102	34	P	ccC/ccT	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=5/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	358	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=3/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	240	102	34	P	ccC/ccT	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1148;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2680;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	241	102	34	P	ccC/ccT	rs11575998,COSV52833841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	352	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	235	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=774;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	238	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	292	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	235	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
818287	17:7676267-7676267	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	245	-	-	-	-	rs11575998,COSV52833841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=4/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=783;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=783;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=783;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1157;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2689;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=783;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=783;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=783;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
752132	17:7676276-7676276	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs746791390,COSV52795451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs35117667	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=785;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs35117667	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=785;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs35117667	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs35117667	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=785;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs35117667	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs35117667	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1159;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs35117667	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2691;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs35117667	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=785;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs35117667	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=785;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs35117667	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=785;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
220942	17:7676278-7676278	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs35117667	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=787;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=787;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=787;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1161;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2693;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=787;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=787;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526841	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=787;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492631	17:7676280-7676280	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526841	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=789;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=789;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597375376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=789;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597375376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1163;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2695;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=789;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=789;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375376	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=789;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
750170	17:7676282-7676282	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1597375376	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=790;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=790;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=790;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1164;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2696;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=790;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=790;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=790;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
380385	17:7676283-7676283	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs769697802,CS011572,COSV52798761	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,0,1;PHENO=1,1,1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526843	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=794;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526843	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=794;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526843	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526843	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=794;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526843	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526843	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1168;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526843	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2700;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526843	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=794;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526843	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=794;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526843	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=794;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
548898	17:7676287-7676287	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526843	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs374547451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=796;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs374547451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=796;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs374547451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs374547451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=796;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs374547451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs374547451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1170;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs374547451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2702;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs374547451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=796;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs374547451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=796;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs374547451	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=796;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
392266	17:7676289-7676289	G	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs374547451	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=798;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=798;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=798;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1172;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2704;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=798;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=798;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=798;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1569628	17:7676291-7676291	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=807;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=807;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=807;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1181;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2713;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=807;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=807;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=807;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
371934	17:7676300-7676300	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs200989844,CS123561	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=808;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=808;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=808;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1182;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2714;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=808;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=808;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=808;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
256604	17:7676301-7676301	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs17883323,COSV99397966	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,1;PHENO=1,1
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1206;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2738;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697625	17:7676324-7676341	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs745875962	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=833;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=833;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=833;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1207;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2739;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=833;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=833;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=833;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
440349	17:7676325-7676341	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1206;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2738;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=832;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
492754	17:7676325-7676325	CCCCAGCCCTCCAGGT	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=833;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=833;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=833;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1207;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2739;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=833;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=833;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=833;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
630717	17:7676325-7676357	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs59758982	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=835;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=835;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=835;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1209;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2741;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=835;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=835;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=835;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
926699	17:7676327-7676351	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=841;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=841;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=841;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1215;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2747;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=841;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=841;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=841;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1679018	17:7676333-7676341	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs780090842	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=842;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=842;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=842;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1216;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2748;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=842;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=842;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=842;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697627	17:7676334-7676340	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=844;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=844;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=844;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1218;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2750;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=844;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=844;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=844;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1697630	17:7676336-7676341	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs776639636	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=848;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=848;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=848;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1222;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2754;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=848;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=848;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=848;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1679019	17:7676341-7676341	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs139100308,COSV99416676	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=851;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=851;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=851;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1225;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2757;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=851;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=851;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=851;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
928156	17:7676344-7676360	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=855;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=855;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=855;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1229;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2761;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=855;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=855;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=855;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492629	17:7676347-7676357	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526882	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1232;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2764;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
182942	17:7676350-7676367	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs730882011	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1232;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2764;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492630	17:7676350-7676351	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526886	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1232;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2764;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629932	17:7676350-7676354	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs773204149	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1233;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2765;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182941	17:7676351-7676367	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs730882010	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1232;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2764;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=858;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
421432	17:7676351-7676367	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1064795134	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1233;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2765;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=859;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
921060	17:7676351-7676364	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=863;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=863;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=863;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1237;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2769;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=863;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=863;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=863;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
629933	17:7676355-7676367	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs765932887	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=871;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=871;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=871;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1245;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2777;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=871;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=871;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=871;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
182943	17:7676363-7676364	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs730882012	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=875;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=875;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=875;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1249;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2781;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=875;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=875;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=875;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492755	17:7676368-7676368	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs757865517	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=877;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=877;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=877;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1251;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2783;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=877;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=877;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=877;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492628	17:7676370-7676370	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs779577884	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=879;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=879;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=879;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1253;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2785;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=879;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=879;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=879;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1105234	17:7676372-7676372	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=880;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=880;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=880;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1254;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2786;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=880;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=880;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=880;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144646	17:7676373-7676373	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=4/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs751183912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=881;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs751183912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=881;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=2/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs751183912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs751183912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=881;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs751183912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1255;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs751183912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2787;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs751183912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=881;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs751183912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=881;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs751183912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=881;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
759310	17:7676374-7676374	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs751183912	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant,splice_region_variant	236	94	32	L/V	Ctg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant,splice_region_variant	94	94	32	L/V	Ctg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant,splice_region_variant	94	94	32	L/V	Ctg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant,splice_region_variant	227	94	32	L/V	Ctg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant,splice_region_variant	230	94	32	L/V	Ctg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant,splice_region_variant	227	94	32	L/V	Ctg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant,splice_region_variant	276	94	32	L/V	Ctg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=891;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=891;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	350	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant,splice_region_variant	232	94	32	L/V	Ctg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=891;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant,splice_region_variant	173	94	32	L/V	Ctg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1265;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2797;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant,splice_region_variant	233	94	32	L/V	Ctg/Gtg	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,5_prime_UTR_variant	344	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,5_prime_UTR_variant	227	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=891;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=891;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=891;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,5_prime_UTR_variant	230	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,5_prime_UTR_variant	284	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,5_prime_UTR_variant	227	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1767161	17:7676384-7676384	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,5_prime_UTR_variant,NMD_transcript_variant	237	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	236	94	32	L	Ctg/Ttg	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,synonymous_variant	94	94	32	L	Ctg/Ttg	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,synonymous_variant	94	94	32	L	Ctg/Ttg	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,synonymous_variant	227	94	32	L	Ctg/Ttg	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	230	94	32	L	Ctg/Ttg	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,synonymous_variant	227	94	32	L	Ctg/Ttg	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,synonymous_variant	276	94	32	L	Ctg/Ttg	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526920	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=891;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526920	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=891;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000505014.5	Transcript	splice_region_variant,non_coding_transcript_exon_variant	350	-	-	-	-	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,synonymous_variant	232	94	32	L	Ctg/Ttg	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526920	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526920	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=891;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,synonymous_variant	173	94	32	L	Ctg/Ttg	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526920	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1265;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526920	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2797;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,synonymous_variant	233	94	32	L	Ctg/Ttg	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000610292.4	Transcript	splice_region_variant,5_prime_UTR_variant	344	-	-	-	-	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,5_prime_UTR_variant	227	-	-	-	-	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526920	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=891;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526920	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=891;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526920	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=891;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,5_prime_UTR_variant	230	-	-	-	-	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,5_prime_UTR_variant	284	-	-	-	-	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,5_prime_UTR_variant	227	-	-	-	-	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
486552	17:7676384-7676384	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,5_prime_UTR_variant,NMD_transcript_variant	237	-	-	-	-	rs1555526920	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	235	93	31	V	gtT/gtG	rs1406108270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	93	93	31	V	gtT/gtG	rs1406108270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	93	93	31	V	gtT/gtG	rs1406108270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	226	93	31	V	gtT/gtG	rs1406108270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	229	93	31	V	gtT/gtG	rs1406108270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	226	93	31	V	gtT/gtG	rs1406108270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	275	93	31	V	gtT/gtG	rs1406108270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	349	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	231	93	31	V	gtT/gtG	rs1406108270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	172	93	31	V	gtT/gtG	rs1406108270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1266;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2798;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	232	93	31	V	gtT/gtG	rs1406108270	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	343	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	226	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=892;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	229	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	283	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	226	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485033	17:7676385-7676385	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	236	-	-	-	-	rs1406108270	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	232	90	30	N	aaC/aaT	rs370992294,COSV53166880,COSV99396148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	90	90	30	N	aaC/aaT	rs370992294,COSV53166880,COSV99396148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	90	90	30	N	aaC/aaT	rs370992294,COSV53166880,COSV99396148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	223	90	30	N	aaC/aaT	rs370992294,COSV53166880,COSV99396148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	226	90	30	N	aaC/aaT	rs370992294,COSV53166880,COSV99396148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	223	90	30	N	aaC/aaT	rs370992294,COSV53166880,COSV99396148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	272	90	30	N	aaC/aaT	rs370992294,COSV53166880,COSV99396148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	346	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	228	90	30	N	aaC/aaT	rs370992294,COSV53166880,COSV99396148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	169	90	30	N	aaC/aaT	rs370992294,COSV53166880,COSV99396148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1269;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2801;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	229	90	30	N	aaC/aaT	rs370992294,COSV53166880,COSV99396148	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	340	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	223	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=895;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	226	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	280	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	223	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
215764	17:7676388-7676388	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	233	-	-	-	-	rs370992294,COSV53166880,COSV99396148	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1,1;PHENO=1,1,1
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	229	87	29	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	87	87	29	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	87	87	29	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	220	87	29	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	223	87	29	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	220	87	29	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	269	87	29	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=898;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=898;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	343	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	225	87	29	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=898;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	166	87	29	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1272;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2804;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	226	87	29	N	aaC/aaT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	337	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	220	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=898;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=898;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=898;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	223	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	277	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	220	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1764717	17:7676391-7676391	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	230	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	227	85	29	N/D	Aac/Gac	rs1597375899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	85	85	29	N/D	Aac/Gac	rs1597375899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	85	85	29	N/D	Aac/Gac	rs1597375899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	218	85	29	N/D	Aac/Gac	rs1597375899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	221	85	29	N/D	Aac/Gac	rs1597375899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	218	85	29	N/D	Aac/Gac	rs1597375899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	267	85	29	N/D	Aac/Gac	rs1597375899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=900;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=900;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	341	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	223	85	29	N/D	Aac/Gac	rs1597375899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=900;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	164	85	29	N/D	Aac/Gac	rs1597375899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1274;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2806;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	224	85	29	N/D	Aac/Gac	rs1597375899	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	335	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	218	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=900;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=900;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=900;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	221	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	275	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	218	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
822586	17:7676393-7676393	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	228	-	-	-	-	rs1597375899	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	223	81	27	P	ccT/ccG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	81	81	27	P	ccT/ccG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	81	81	27	P	ccT/ccG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	214	81	27	P	ccT/ccG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	217	81	27	P	ccT/ccG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	214	81	27	P	ccT/ccG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	263	81	27	P	ccT/ccG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	337	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	219	81	27	P	ccT/ccG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	160	81	27	P	ccT/ccG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1278;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2810;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	220	81	27	P	ccT/ccG	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	331	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	214	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	217	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	271	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	214	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1762440	17:7676397-7676397	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	224	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	223	81	27	P	ccT/ccC	rs1555526932	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	81	81	27	P	ccT/ccC	rs1555526932	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	81	81	27	P	ccT/ccC	rs1555526932	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	214	81	27	P	ccT/ccC	rs1555526932	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	217	81	27	P	ccT/ccC	rs1555526932	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	214	81	27	P	ccT/ccC	rs1555526932	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	263	81	27	P	ccT/ccC	rs1555526932	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	337	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	219	81	27	P	ccT/ccC	rs1555526932	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	160	81	27	P	ccT/ccC	rs1555526932	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1278;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2810;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	220	81	27	P	ccT/ccC	rs1555526932	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	331	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	214	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=904;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	217	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	214	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
511134	17:7676397-7676397	G	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	224	-	-	-	-	rs1555526932	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	220	78	26	L	ctT/ctC	rs934176141,CD1610077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	78	78	26	L	ctT/ctC	rs934176141,CD1610077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	78	78	26	L	ctT/ctC	rs934176141,CD1610077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	211	78	26	L	ctT/ctC	rs934176141,CD1610077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	214	78	26	L	ctT/ctC	rs934176141,CD1610077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	211	78	26	L	ctT/ctC	rs934176141,CD1610077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	260	78	26	L	ctT/ctC	rs934176141,CD1610077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=4/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=907;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=907;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	334	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	216	78	26	L	ctT/ctC	rs934176141,CD1610077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=907;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	157	78	26	L	ctT/ctC	rs934176141,CD1610077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1281;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2813;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	217	78	26	L	ctT/ctC	rs934176141,CD1610077	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	328	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	211	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=907;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=907;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=907;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	214	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	268	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	211	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
482209	17:7676400-7676400	G	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	221	-	-	-	-	rs934176141,CD1610077	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1,1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1051425969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=922;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1051425969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=922;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	319	-	-	-	-	rs1051425969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1051425969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1051425969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=922;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1051425969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1296;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1051425969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2828;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	313	-	-	-	-	rs1051425969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1051425969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=922;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1051425969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=922;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1051425969	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=922;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1051425969	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492601	17:7676415-7676415	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1051425969	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs747908393	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=924;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs747908393	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=924;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	317	-	-	-	-	rs747908393	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs747908393	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs747908393	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=924;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs747908393	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1298;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs747908393	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2830;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	311	-	-	-	-	rs747908393	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs747908393	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=924;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs747908393	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=924;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs747908393	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=924;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs747908393	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
380318	17:7676417-7676417	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs747908393	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=925;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=925;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	316	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=925;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1299;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2831;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	310	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=925;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=925;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=925;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1548802	17:7676418-7676418	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=enhancer
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=926;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=926;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	315	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=926;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1300;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2832;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	309	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=926;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=926;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=926;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1616173	17:7676419-7676419	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=enhancer
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs910296194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=927;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs910296194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=927;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	314	-	-	-	-	rs910296194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs910296194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs910296194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=927;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs910296194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1301;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs910296194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2833;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	308	-	-	-	-	rs910296194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs910296194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=927;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs910296194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=927;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs910296194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=927;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs910296194	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492602	17:7676420-7676420	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs910296194	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=928;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=928;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	313	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=928;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1302;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2834;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	307	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=928;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=928;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=928;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
492603	17:7676421-7676421	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1273569924	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=benign,likely_benign;PHENO=1
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=929;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=929;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	312	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=929;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1303;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2835;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	306	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=929;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=929;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=929;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1542745	17:7676422-7676422	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=enhancer
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=937;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=937;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	304	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=937;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1311;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2843;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	298	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=937;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=937;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=937;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492604	17:7676430-7676430	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs943163238	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=940;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=940;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	301	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=940;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1314;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2846;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	295	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=940;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=940;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=940;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629934	17:7676433-7676433	G	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs368444215	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=941;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=941;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	300	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=941;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1315;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2847;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	294	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=941;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=941;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=941;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628762	17:7676434-7676434	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567557800	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=942;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=942;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	299	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=942;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1316;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2848;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	293	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=942;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=942;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=942;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630546	17:7676435-7676435	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs745951235	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=950;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=950;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	291	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=950;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1324;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2856;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	285	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=950;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=950;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=950;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492605	17:7676443-7676443	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs372756865	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=951;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=951;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	290	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=951;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1325;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2857;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	284	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=951;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=951;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=951;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492606	17:7676444-7676444	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs569425726	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=952;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=952;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	289	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=952;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1326;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2858;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	283	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=952;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=952;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=952;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492607	17:7676445-7676445	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs768964728	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=953;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=953;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	288	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=953;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1327;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2859;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	282	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=953;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=953;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=953;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630512	17:7676446-7676446	G	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs762253412,COSV52998357	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=957;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=957;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	284	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=957;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1331;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2863;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	278	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=957;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=957;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=957;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
630590	17:7676450-7676450	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs765673441	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=959;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=959;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	282	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=959;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1333;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2865;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	276	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=959;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=959;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=959;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492608	17:7676452-7676452	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555526952	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=964;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=964;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	277	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=964;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1338;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2870;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	271	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=964;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=964;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=964;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492609	17:7676457-7676457	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs971879465	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=966;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=966;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	275	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=966;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1340;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2872;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	269	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=966;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=966;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=966;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492610	17:7676459-7676459	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1364767238	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=969;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=969;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	272	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=969;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1343;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2875;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	266	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=969;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=969;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=969;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492600	17:7676462-7676462	G	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555526955	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	270	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1345;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2877;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	264	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492599	17:7676463-7676464	-	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555526956	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	269-270	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1345;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2877;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	263-264	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=971;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628384	17:7676464-7676464	GGGGGCTGGGGTTGGGGT	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567557864	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	269	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1346;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2878;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	263	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492598	17:7676465-7676465	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555526957	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	268-269	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1346;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2878;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	262-263	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=972;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918318	17:7676465-7676465	GGGGCT	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=enhancer
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=974;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=974;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	267	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=974;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1348;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2880;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	261	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=974;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=974;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=974;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
629398	17:7676467-7676467	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567557870	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=980;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=980;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	261	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=980;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1354;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2886;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	255	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=980;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=980;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=980;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927973	17:7676473-7676473	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs765863585	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	259	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1356;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2888;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	253	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1697637	17:7676475-7676475	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV52802912	IMPACT=MODIFIER;BIOTYPE=enhancer;SOMATIC=1;PHENO=1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	259	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1356;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2888;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	253	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=982;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
925769	17:7676475-7676475	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1356817780,COSV52802912	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=984;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=984;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	257	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=984;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1358;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2890;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	251	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=984;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=984;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=984;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492597	17:7676477-7676477	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs377074538,COSV53060246	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=987;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=987;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	254	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=987;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1361;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2893;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	248	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=987;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=987;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=987;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492596	17:7676480-7676480	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs752547878	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	251	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1364;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2896;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	245	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
137691	17:7676483-7676483	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	251	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1364;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2896;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	245	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
492595	17:7676483-7676483	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1642785,CR1413385,COSV52668860	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=benign;SOMATIC=0,0,1;PHENO=1,1,1
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	250-251	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1364;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2896;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	244-245	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=990;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
918941	17:7676483-7676484	CA	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=enhancer
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=991;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=991;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	250	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=991;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1365;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2897;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	244	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=991;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=991;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=991;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492594	17:7676484-7676484	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs749212949,COSV53555935	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=993;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=993;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	248	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=993;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1367;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2899;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	242	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=993;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=993;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=993;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492593	17:7676486-7676486	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs984971583	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=994;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=994;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	247	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=994;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1368;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2900;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	241	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=994;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=994;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=994;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
628567	17:7676487-7676487	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs758434025	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=996;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=996;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	245	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=996;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1370;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2902;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	239	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=996;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=996;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=996;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
629294	17:7676489-7676489	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1567557970,COSV53597375	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=999;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=999;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	240-242	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=999;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1373;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2905;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	234-236	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=999;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=999;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=999;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492591	17:7676491-7676494	-	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1167199080	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=998;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=998;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	243	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=998;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1372;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2904;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	237	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=998;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=998;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=998;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
922250	17:7676491-7676491	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597376305	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1000;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1000;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	241	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1000;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1374;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2906;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	235	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1000;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1000;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1000;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
927956	17:7676493-7676493	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1187025137	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1001;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1001;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	240	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1001;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1375;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2907;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	234	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1001;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1001;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1001;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492592	17:7676494-7676494	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555526978	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1004;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1004;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	237	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1004;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1378;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2910;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	231	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1004;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1004;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1004;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
920224	17:7676497-7676497	G	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2073516973	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1005;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1005;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	236	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1005;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1379;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2911;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	230	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1005;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1005;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1005;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1696412	17:7676498-7676498	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1453148314	IMPACT=MODIFIER;BIOTYPE=enhancer
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1006;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1006;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	235	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1006;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1380;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2912;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	229	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1006;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1006;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1006;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
492590	17:7676499-7676499	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs780218773	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1011;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1011;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	230	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1011;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1385;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2917;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	224	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1011;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1011;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1011;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1562027	17:7676504-7676504	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=enhancer
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1014;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1014;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	227	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1014;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1388;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2920;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	221	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1014;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1014;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1014;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
372044	17:7676507-7676507	G	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs184743157	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=benign,likely_benign;PHENO=1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1016;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1016;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	225	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1016;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1390;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2922;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	219	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1016;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1016;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1016;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922868	17:7676509-7676509	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2073517739,COSV53551708	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000359597.8	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000413465.6	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1018;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1018;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	223	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1018;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1392;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2924;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	217	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1018;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1018;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1018;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1112878	17:7676511-7676511	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs769054558	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs776933919	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1020;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs776933919	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1020;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	221	-	-	-	-	rs776933919	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs776933919	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs776933919	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1020;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs776933919	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1394;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs776933919	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2926;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	215	-	-	-	-	rs776933919	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs776933919	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1020;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs776933919	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1020;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs776933919	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1020;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs776933919	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
458561	17:7676513-7676513	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs776933919	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/6;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=3/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376387	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1021;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376387	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1021;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	220	-	-	-	-	rs1597376387	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1597376387	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376387	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1021;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376387	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1395;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376387	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2927;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	214	-	-	-	-	rs1597376387	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376387	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1021;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376387	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1021;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1597376387	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1021;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,intron_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1597376387	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
756368	17:7676514-7676514	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1597376387	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_region_variant,synonymous_variant	214	72	24	K	aaA/aaG	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000359597.8	Transcript	splice_region_variant,synonymous_variant	72	72	24	K	aaA/aaG	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000413465.6	Transcript	splice_region_variant,synonymous_variant	72	72	24	K	aaA/aaG	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_region_variant,synonymous_variant	205	72	24	K	aaA/aaG	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_region_variant,synonymous_variant	208	72	24	K	aaA/aaG	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_region_variant,synonymous_variant	205	72	24	K	aaA/aaG	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_region_variant,synonymous_variant	254	72	24	K	aaA/aaG	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	211	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_region_variant,synonymous_variant	210	72	24	K	aaA/aaG	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_region_variant,synonymous_variant	151	72	24	K	aaA/aaG	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1404;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2936;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000604348.5	Transcript	splice_region_variant,synonymous_variant	211	72	24	K	aaA/aaG	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	205	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_region_variant,5_prime_UTR_variant	205	-	-	-	-	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1030;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_region_variant,5_prime_UTR_variant	208	-	-	-	-	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_region_variant,5_prime_UTR_variant	262	-	-	-	-	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_region_variant,5_prime_UTR_variant	205	-	-	-	-	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_region_variant,5_prime_UTR_variant,NMD_transcript_variant	215	-	-	-	-	CD137623	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;PHENO=1
1758175	17:7676523-7676523	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	CD137623	IMPACT=MODIFIER;BIOTYPE=enhancer;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	202	60	20	S	tcA/tcG	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	60	60	20	S	tcA/tcG	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	60	60	20	S	tcA/tcG	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	193	60	20	S	tcA/tcG	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	196	60	20	S	tcA/tcG	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	193	60	20	S	tcA/tcG	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	242	60	20	S	tcA/tcG	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1042;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1042;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	199	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	198	60	20	S	tcA/tcG	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1042;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	139	60	20	S	tcA/tcG	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1416;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2948;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	199	60	20	S	tcA/tcG	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	193	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	193	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1042;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1042;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1042;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	196	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	250	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	193	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	203	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
184872	17:7676535-7676535	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	202	60	20	S	tcA/tcT	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	60	60	20	S	tcA/tcT	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	60	60	20	S	tcA/tcT	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	193	60	20	S	tcA/tcT	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	196	60	20	S	tcA/tcT	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	193	60	20	S	tcA/tcT	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	242	60	20	S	tcA/tcT	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1042;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1042;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	199	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	198	60	20	S	tcA/tcT	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1042;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	139	60	20	S	tcA/tcT	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1416;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2948;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	199	60	20	S	tcA/tcT	rs786201754	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	193	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	193	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1042;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1042;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1042;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	196	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	250	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	193	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	203	-	-	-	-	rs786201754	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
762200	17:7676535-7676535	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs786201754	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	199	57	19	F	ttT/ttC	rs763565673	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	57	57	19	F	ttT/ttC	rs763565673	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	57	57	19	F	ttT/ttC	rs763565673	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	190	57	19	F	ttT/ttC	rs763565673	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	193	57	19	F	ttT/ttC	rs763565673	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	190	57	19	F	ttT/ttC	rs763565673	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	239	57	19	F	ttT/ttC	rs763565673	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1045;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1045;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	196	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	195	57	19	F	ttT/ttC	rs763565673	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1045;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	136	57	19	F	ttT/ttC	rs763565673	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1419;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2951;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	196	57	19	F	ttT/ttC	rs763565673	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	190	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	190	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1045;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1045;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1045;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	193	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	247	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	190	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	200	-	-	-	-	rs763565673	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
755248	17:7676538-7676538	G	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs763565673	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	196	54	18	T	acA/acG	rs876659984,COSV53717001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	54	54	18	T	acA/acG	rs876659984,COSV53717001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	54	54	18	T	acA/acG	rs876659984,COSV53717001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	187	54	18	T	acA/acG	rs876659984,COSV53717001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	190	54	18	T	acA/acG	rs876659984,COSV53717001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	187	54	18	T	acA/acG	rs876659984,COSV53717001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	236	54	18	T	acA/acG	rs876659984,COSV53717001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1048;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1048;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	193	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	192	54	18	T	acA/acG	rs876659984,COSV53717001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1048;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	133	54	18	T	acA/acG	rs876659984,COSV53717001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1422;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2954;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	193	54	18	T	acA/acG	rs876659984,COSV53717001	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	187	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	187	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1048;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1048;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1048;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	190	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	244	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	187	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	197	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
232776	17:7676541-7676541	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs876659984,COSV53717001	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	187	45	15	S	agT/agC	rs766765429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	45	45	15	S	agT/agC	rs766765429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	45	45	15	S	agT/agC	rs766765429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	178	45	15	S	agT/agC	rs766765429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	181	45	15	S	agT/agC	rs766765429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	178	45	15	S	agT/agC	rs766765429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	227	45	15	S	agT/agC	rs766765429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	184	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	183	45	15	S	agT/agC	rs766765429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	124	45	15	S	agT/agC	rs766765429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1431;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2963;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	184	45	15	S	agT/agC	rs766765429	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	178	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	178	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1057;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	181	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	235	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	178	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	188	-	-	-	-	rs766765429	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414036	17:7676550-7676550	G	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs766765429	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	184	42	14	L	ctG/ctC	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	42	42	14	L	ctG/ctC	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	42	42	14	L	ctG/ctC	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	175	42	14	L	ctG/ctC	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	178	42	14	L	ctG/ctC	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	175	42	14	L	ctG/ctC	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	224	42	14	L	ctG/ctC	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1060;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1060;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	181	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	180	42	14	L	ctG/ctC	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1060;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	121	42	14	L	ctG/ctC	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1434;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2966;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	181	42	14	L	ctG/ctC	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	175	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	175	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1060;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1060;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1060;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	178	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	232	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	175	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	185	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
187075	17:7676553-7676553	G	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	184	42	14	L	ctG/ctA	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	42	42	14	L	ctG/ctA	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	42	42	14	L	ctG/ctA	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	175	42	14	L	ctG/ctA	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	178	42	14	L	ctG/ctA	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	175	42	14	L	ctG/ctA	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	224	42	14	L	ctG/ctA	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1060;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1060;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	181	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	180	42	14	L	ctG/ctA	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1060;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	121	42	14	L	ctG/ctA	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1434;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2966;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	181	42	14	L	ctG/ctA	rs773918872,COSV99356235	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	175	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	175	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1060;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1060;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1060;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	178	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	232	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	175	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	185	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
824769	17:7676553-7676553	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs773918872,COSV99356235	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	182	40	14	L	Ctg/Ttg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	40	40	14	L	Ctg/Ttg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	40	40	14	L	Ctg/Ttg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	173	40	14	L	Ctg/Ttg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	176	40	14	L	Ctg/Ttg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	173	40	14	L	Ctg/Ttg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	222	40	14	L	Ctg/Ttg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1062;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1062;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	179	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	178	40	14	L	Ctg/Ttg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1062;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	119	40	14	L	Ctg/Ttg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1436;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2968;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	179	40	14	L	Ctg/Ttg	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	173	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	173	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1062;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1062;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1062;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	176	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	230	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	173	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	183	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1086881	17:7676555-7676555	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=enhancer
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	181	39	13	P	ccT/ccG	rs1555527000	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	39	39	13	P	ccT/ccG	rs1555527000	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	39	39	13	P	ccT/ccG	rs1555527000	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	172	39	13	P	ccT/ccG	rs1555527000	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	175	39	13	P	ccT/ccG	rs1555527000	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	172	39	13	P	ccT/ccG	rs1555527000	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	221	39	13	P	ccT/ccG	rs1555527000	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1063;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1063;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	178	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	177	39	13	P	ccT/ccG	rs1555527000	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1063;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	118	39	13	P	ccT/ccG	rs1555527000	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1437;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2969;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	178	39	13	P	ccT/ccG	rs1555527000	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	172	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	172	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1063;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1063;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1063;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	175	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	229	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	172	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	182	-	-	-	-	rs1555527000	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
482227	17:7676556-7676556	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555527000	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	179	37	13	P/A	Cct/Gct	COSV53056194	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	37	37	13	P/A	Cct/Gct	COSV53056194	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	37	37	13	P/A	Cct/Gct	COSV53056194	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	170	37	13	P/A	Cct/Gct	COSV53056194	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	173	37	13	P/A	Cct/Gct	COSV53056194	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	170	37	13	P/A	Cct/Gct	COSV53056194	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	219	37	13	P/A	Cct/Gct	COSV53056194	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1065;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1065;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	176	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	175	37	13	P/A	Cct/Gct	COSV53056194	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1065;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	116	37	13	P/A	Cct/Gct	COSV53056194	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1439;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2971;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	176	37	13	P/A	Cct/Gct	COSV53056194	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	170	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	170	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1065;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1065;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1065;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	173	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	227	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	170	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	180	-	-	-	-	COSV53056194	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1;PHENO=1
1735038	17:7676558-7676558	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV53056194	IMPACT=MODIFIER;BIOTYPE=enhancer;SOMATIC=1;PHENO=1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	178	36	12	P	ccC/ccT	rs767173379,COSV105016287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	36	36	12	P	ccC/ccT	rs767173379,COSV105016287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	36	36	12	P	ccC/ccT	rs767173379,COSV105016287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	169	36	12	P	ccC/ccT	rs767173379,COSV105016287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	172	36	12	P	ccC/ccT	rs767173379,COSV105016287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	169	36	12	P	ccC/ccT	rs767173379,COSV105016287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	218	36	12	P	ccC/ccT	rs767173379,COSV105016287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1066;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1066;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	175	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	174	36	12	P	ccC/ccT	rs767173379,COSV105016287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1066;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	115	36	12	P	ccC/ccT	rs767173379,COSV105016287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1440;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2972;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	175	36	12	P	ccC/ccT	rs767173379,COSV105016287	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	169	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	169	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1066;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1066;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1066;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	172	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	226	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	169	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	179	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1127673	17:7676559-7676559	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs767173379,COSV105016287	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	175	33	11	E	gaG/gaA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	33	33	11	E	gaG/gaA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	33	33	11	E	gaG/gaA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	166	33	11	E	gaG/gaA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	169	33	11	E	gaG/gaA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	166	33	11	E	gaG/gaA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	215	33	11	E	gaG/gaA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1069;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1069;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	172	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	171	33	11	E	gaG/gaA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1069;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	112	33	11	E	gaG/gaA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1443;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2975;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	172	33	11	E	gaG/gaA	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	166	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	166	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1069;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1069;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1069;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	169	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	223	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	166	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	176	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1638746	17:7676562-7676562	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=enhancer
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	172	30	10	V	gtC/gtT	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	30	30	10	V	gtC/gtT	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	30	30	10	V	gtC/gtT	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	163	30	10	V	gtC/gtT	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	166	30	10	V	gtC/gtT	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	163	30	10	V	gtC/gtT	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	212	30	10	V	gtC/gtT	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1072;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1072;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	169	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	168	30	10	V	gtC/gtT	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1072;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	109	30	10	V	gtC/gtT	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2978;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	169	30	10	V	gtC/gtT	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	163	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	163	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1072;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1072;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1072;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	166	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	220	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	163	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	173	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
183952	17:7676565-7676565	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	172	30	10	V	gtC/gtG	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	30	30	10	V	gtC/gtG	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	30	30	10	V	gtC/gtG	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	163	30	10	V	gtC/gtG	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	166	30	10	V	gtC/gtG	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	163	30	10	V	gtC/gtG	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	212	30	10	V	gtC/gtG	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1072;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1072;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	169	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	168	30	10	V	gtC/gtG	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1072;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	109	30	10	V	gtC/gtG	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2978;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	169	30	10	V	gtC/gtG	rs568171603,COSV52910540	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	163	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	163	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1072;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1072;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1072;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	166	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	220	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	163	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	173	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
458534	17:7676565-7676565	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs568171603,COSV52910540	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	170	28	10	V/L	Gtc/Ctc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	28	28	10	V/L	Gtc/Ctc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	28	28	10	V/L	Gtc/Ctc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	161	28	10	V/L	Gtc/Ctc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	164	28	10	V/L	Gtc/Ctc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	161	28	10	V/L	Gtc/Ctc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	210	28	10	V/L	Gtc/Ctc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	167	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	166	28	10	V/L	Gtc/Ctc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	107	28	10	V/L	Gtc/Ctc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1448;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2980;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	167	28	10	V/L	Gtc/Ctc	rs535274413,COSV52756545	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	161	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	161	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1074;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	164	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	218	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	161	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	171	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
231387	17:7676567-7676567	G	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs535274413,COSV52756545	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=conflicting_interpretations_of_pathogenicity,uncertain_significance,likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	169	27	9	S	agC/agT	rs757282628,COSV99384830	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	27	27	9	S	agC/agT	rs757282628,COSV99384830	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	27	27	9	S	agC/agT	rs757282628,COSV99384830	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	160	27	9	S	agC/agT	rs757282628,COSV99384830	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	163	27	9	S	agC/agT	rs757282628,COSV99384830	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	160	27	9	S	agC/agT	rs757282628,COSV99384830	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	209	27	9	S	agC/agT	rs757282628,COSV99384830	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1075;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1075;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	166	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	165	27	9	S	agC/agT	rs757282628,COSV99384830	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1075;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	106	27	9	S	agC/agT	rs757282628,COSV99384830	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1449;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2981;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	166	27	9	S	agC/agT	rs757282628,COSV99384830	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	160	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	160	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1075;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1075;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1075;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	163	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	217	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	160	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	170	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
215762	17:7676568-7676568	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs757282628,COSV99384830	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	165	23	8	P/R	cCt/cGt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	23	23	8	P/R	cCt/cGt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	23	23	8	P/R	cCt/cGt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	156	23	8	P/R	cCt/cGt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	159	23	8	P/R	cCt/cGt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	156	23	8	P/R	cCt/cGt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	205	23	8	P/R	cCt/cGt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1079;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1079;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	162	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	161	23	8	P/R	cCt/cGt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1079;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	102	23	8	P/R	cCt/cGt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1453;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2985;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	162	23	8	P/R	cCt/cGt	-	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	156	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	156	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1079;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1079;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1079;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	159	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	213	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	156	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	166	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1790705	17:7676572-7676572	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=enhancer
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	165	23	8	P/L	cCt/cTt	rs876659415	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	23	23	8	P/L	cCt/cTt	rs876659415	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	23	23	8	P/L	cCt/cTt	rs876659415	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	156	23	8	P/L	cCt/cTt	rs876659415	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	159	23	8	P/L	cCt/cTt	rs876659415	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	156	23	8	P/L	cCt/cTt	rs876659415	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	205	23	8	P/L	cCt/cTt	rs876659415	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1079;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1079;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	162	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	161	23	8	P/L	cCt/cTt	rs876659415	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1079;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	102	23	8	P/L	cCt/cTt	rs876659415	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1453;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2985;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	162	23	8	P/L	cCt/cTt	rs876659415	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	156	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	156	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1079;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1079;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1079;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	159	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	213	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	156	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	166	-	-	-	-	rs876659415	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
231868	17:7676572-7676572	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs876659415	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	163	21	7	D/E	gaT/gaA	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	21	21	7	D/E	gaT/gaA	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	21	21	7	D/E	gaT/gaA	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	154	21	7	D/E	gaT/gaA	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	157	21	7	D/E	gaT/gaA	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	154	21	7	D/E	gaT/gaA	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	203	21	7	D/E	gaT/gaA	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1081;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1081;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	160	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	159	21	7	D/E	gaT/gaA	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1081;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	100	21	7	D/E	gaT/gaA	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1455;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2987;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	160	21	7	D/E	gaT/gaA	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	154	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	154	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1081;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1081;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1081;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	157	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	211	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	154	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	164	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
140782	17:7676574-7676574	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=uncertain_significance,conflicting_interpretations_of_pathogenicity,likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	163	21	7	D/E	gaT/gaG	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	21	21	7	D/E	gaT/gaG	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	21	21	7	D/E	gaT/gaG	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	154	21	7	D/E	gaT/gaG	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	157	21	7	D/E	gaT/gaG	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	154	21	7	D/E	gaT/gaG	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	203	21	7	D/E	gaT/gaG	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1081;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1081;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	160	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	159	21	7	D/E	gaT/gaG	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1081;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	100	21	7	D/E	gaT/gaG	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1455;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2987;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	160	21	7	D/E	gaT/gaG	rs587781277	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	154	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	154	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1081;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1081;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1081;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	157	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	211	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	154	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	164	-	-	-	-	rs587781277	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
485049	17:7676574-7676574	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs587781277	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	160	18	6	S	tcA/tcC	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	18	18	6	S	tcA/tcC	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	18	18	6	S	tcA/tcC	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	151	18	6	S	tcA/tcC	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	154	18	6	S	tcA/tcC	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	151	18	6	S	tcA/tcC	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	200	18	6	S	tcA/tcC	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1084;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1084;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	157	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	156	18	6	S	tcA/tcC	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1084;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	97	18	6	S	tcA/tcC	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1458;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2990;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	157	18	6	S	tcA/tcC	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	151	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	151	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1084;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1084;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1084;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	154	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	208	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	151	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	161	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
182940	17:7676577-7676577	G	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=benign/likely_benign,likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	160	18	6	S	tcA/tcG	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	18	18	6	S	tcA/tcG	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	18	18	6	S	tcA/tcG	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	151	18	6	S	tcA/tcG	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	154	18	6	S	tcA/tcG	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	151	18	6	S	tcA/tcG	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	200	18	6	S	tcA/tcG	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1084;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1084;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	157	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	156	18	6	S	tcA/tcG	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1084;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	97	18	6	S	tcA/tcG	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1458;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2990;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	157	18	6	S	tcA/tcG	rs573130482	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	151	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	151	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1084;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1084;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1084;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	154	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	208	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	151	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	161	-	-	-	-	rs573130482	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
414037	17:7676577-7676577	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs573130482	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	157	15	5	Q	caG/caA	COSV106055434,COSV53772032	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	15	15	5	Q	caG/caA	COSV106055434,COSV53772032	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	15	15	5	Q	caG/caA	COSV106055434,COSV53772032	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	148	15	5	Q	caG/caA	COSV106055434,COSV53772032	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	151	15	5	Q	caG/caA	COSV106055434,COSV53772032	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	148	15	5	Q	caG/caA	COSV106055434,COSV53772032	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	197	15	5	Q	caG/caA	COSV106055434,COSV53772032	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1087;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1087;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	154	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	153	15	5	Q	caG/caA	COSV106055434,COSV53772032	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1087;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	94	15	5	Q	caG/caA	COSV106055434,COSV53772032	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1461;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2993;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	154	15	5	Q	caG/caA	COSV106055434,COSV53772032	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	148	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	148	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1087;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1087;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1087;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	151	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	205	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	148	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	158	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;SOMATIC=1,1;PHENO=1,1
1140062	17:7676580-7676580	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	COSV106055434,COSV53772032	IMPACT=MODIFIER;BIOTYPE=enhancer;SOMATIC=1,1;PHENO=1,1
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	154	12	4	P	ccG/ccT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	12	12	4	P	ccG/ccT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	12	12	4	P	ccG/ccT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	145	12	4	P	ccG/ccT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	148	12	4	P	ccG/ccT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	145	12	4	P	ccG/ccT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	194	12	4	P	ccG/ccT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	151	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	150	12	4	P	ccG/ccT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	91	12	4	P	ccG/ccT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1464;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2996;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	151	12	4	P	ccG/ccT	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	145	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	145	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	148	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	202	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	145	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	155	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1080351	17:7676583-7676583	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=enhancer
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	154	12	4	P	ccG/ccC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	12	12	4	P	ccG/ccC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	12	12	4	P	ccG/ccC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	145	12	4	P	ccG/ccC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	148	12	4	P	ccG/ccC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	145	12	4	P	ccG/ccC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	194	12	4	P	ccG/ccC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	151	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	150	12	4	P	ccG/ccC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	91	12	4	P	ccG/ccC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1464;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2996;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	151	12	4	P	ccG/ccC	-	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	145	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	145	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	148	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	202	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	145	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	155	-	-	-	-	-	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1144950	17:7676583-7676583	G	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	-	IMPACT=MODIFIER;BIOTYPE=enhancer
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	154	12	4	P	ccG/ccA	rs876658274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	12	12	4	P	ccG/ccA	rs876658274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	12	12	4	P	ccG/ccA	rs876658274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	145	12	4	P	ccG/ccA	rs876658274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	148	12	4	P	ccG/ccA	rs876658274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	145	12	4	P	ccG/ccA	rs876658274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	194	12	4	P	ccG/ccA	rs876658274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	151	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	150	12	4	P	ccG/ccA	rs876658274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	91	12	4	P	ccG/ccA	rs876658274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1464;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2996;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	151	12	4	P	ccG/ccA	rs876658274	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	145	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	145	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1090;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	148	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	202	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	145	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	155	-	-	-	-	rs876658274	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
229927	17:7676583-7676583	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs876658274	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000269305.9	Transcript	missense_variant	153	11	4	P/L	cCg/cTg	rs878854064,COSV52800363	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000359597.8	Transcript	missense_variant	11	11	4	P/L	cCg/cTg	rs878854064,COSV52800363	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000413465.6	Transcript	missense_variant	11	11	4	P/L	cCg/cTg	rs878854064,COSV52800363	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000420246.6	Transcript	missense_variant	144	11	4	P/L	cCg/cTg	rs878854064,COSV52800363	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000445888.6	Transcript	missense_variant	147	11	4	P/L	cCg/cTg	rs878854064,COSV52800363	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000455263.6	Transcript	missense_variant	144	11	4	P/L	cCg/cTg	rs878854064,COSV52800363	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000503591.1	Transcript	missense_variant	193	11	4	P/L	cCg/cTg	rs878854064,COSV52800363	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1091;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1091;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	150	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000508793.5	Transcript	missense_variant	149	11	4	P/L	cCg/cTg	rs878854064,COSV52800363	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1091;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000514944.5	Transcript	missense_variant	90	11	4	P/L	cCg/cTg	rs878854064,COSV52800363	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1465;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2997;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000604348.5	Transcript	missense_variant	150	11	4	P/L	cCg/cTg	rs878854064,COSV52800363	IMPACT=MODERATE;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	144	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	144	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1091;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1091;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1091;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	147	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	201	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	144	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	154	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
237941	17:7676584-7676584	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs878854064,COSV52800363	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign,uncertain_significance;SOMATIC=0,1;PHENO=1,1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	151	9	3	E	gaG/gaA	rs1555527028	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	9	9	3	E	gaG/gaA	rs1555527028	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	9	9	3	E	gaG/gaA	rs1555527028	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	142	9	3	E	gaG/gaA	rs1555527028	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	145	9	3	E	gaG/gaA	rs1555527028	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	142	9	3	E	gaG/gaA	rs1555527028	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	191	9	3	E	gaG/gaA	rs1555527028	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1093;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1093;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	148	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	147	9	3	E	gaG/gaA	rs1555527028	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1093;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	88	9	3	E	gaG/gaA	rs1555527028	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1467;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=2999;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	148	9	3	E	gaG/gaA	rs1555527028	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	142	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	142	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1093;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1093;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1093;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	145	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	199	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	142	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	152	-	-	-	-	rs1555527028	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
506486	17:7676586-7676586	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555527028	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000269305.9	Transcript	synonymous_variant	148	6	2	E	gaG/gaA	rs143458271	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000359597.8	Transcript	synonymous_variant	6	6	2	E	gaG/gaA	rs143458271	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000413465.6	Transcript	synonymous_variant	6	6	2	E	gaG/gaA	rs143458271	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/7;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000420246.6	Transcript	synonymous_variant	139	6	2	E	gaG/gaA	rs143458271	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000445888.6	Transcript	synonymous_variant	142	6	2	E	gaG/gaA	rs143458271	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000455263.6	Transcript	synonymous_variant	139	6	2	E	gaG/gaA	rs143458271	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000503591.1	Transcript	synonymous_variant	188	6	2	E	gaG/gaA	rs143458271	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1096;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1096;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	145	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000508793.5	Transcript	synonymous_variant	144	6	2	E	gaG/gaA	rs143458271	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1096;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000514944.5	Transcript	synonymous_variant	85	6	2	E	gaG/gaA	rs143458271	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1470;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3002;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000604348.5	Transcript	synonymous_variant	145	6	2	E	gaG/gaA	rs143458271	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	139	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	139	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1096;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1096;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1096;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	142	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	196	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	139	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	149	-	-	-	-	rs143458271	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
183836	17:7676589-7676589	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs143458271	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=benign,likely_benign,benign/likely_benign;PHENO=1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000269305.9	Transcript	5_prime_UTR_variant	132	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000359597.8	Transcript	upstream_gene_variant	-	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000413465.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000420246.6	Transcript	5_prime_UTR_variant	123	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000445888.6	Transcript	5_prime_UTR_variant	126	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000455263.6	Transcript	5_prime_UTR_variant	123	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000503591.1	Transcript	5_prime_UTR_variant	172	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1112;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1112;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	129	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000508793.5	Transcript	5_prime_UTR_variant	128	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1112;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000514944.5	Transcript	5_prime_UTR_variant	69	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1486;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3018;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000604348.5	Transcript	5_prime_UTR_variant	129	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	123	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	123	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1112;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1112;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1112;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	126	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	180	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	123	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	133	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
922026	17:7676605-7676605	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs773666793,COSV105025854	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000269305.9	Transcript	5_prime_UTR_variant	131	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000359597.8	Transcript	upstream_gene_variant	-	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000413465.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000420246.6	Transcript	5_prime_UTR_variant	122	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000445888.6	Transcript	5_prime_UTR_variant	125	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000455263.6	Transcript	5_prime_UTR_variant	122	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000503591.1	Transcript	5_prime_UTR_variant	171	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1113;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1113;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	128	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000508793.5	Transcript	5_prime_UTR_variant	127	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1113;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000514944.5	Transcript	5_prime_UTR_variant	68	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1487;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3019;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000604348.5	Transcript	5_prime_UTR_variant	128	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	122	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	122	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1113;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1113;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1113;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	125	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	179	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	122	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	132	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
389752	17:7676606-7676606	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs375229869,COSV52971355	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000269305.9	Transcript	5_prime_UTR_variant	127	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000359597.8	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=16;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000413465.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=16;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000420246.6	Transcript	5_prime_UTR_variant	118	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000445888.6	Transcript	5_prime_UTR_variant	121	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000455263.6	Transcript	5_prime_UTR_variant	118	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000503591.1	Transcript	5_prime_UTR_variant	167	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1117;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1117;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	124	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000508793.5	Transcript	5_prime_UTR_variant	123	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1117;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000514944.5	Transcript	5_prime_UTR_variant	64	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1491;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3023;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000604348.5	Transcript	5_prime_UTR_variant	124	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	118	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	118	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1117;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1117;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1117;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	121	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	175	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	118	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	128	-	-	-	-	rs1057520385	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
378743	17:7676610-7676610	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057520385	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000269305.9	Transcript	5_prime_UTR_variant	123	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000359597.8	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=20;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000413465.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=20;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000420246.6	Transcript	5_prime_UTR_variant	114	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000445888.6	Transcript	5_prime_UTR_variant	117	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000455263.6	Transcript	5_prime_UTR_variant	114	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000503591.1	Transcript	5_prime_UTR_variant	163	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=3/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1121;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1121;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	120	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=2/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000508793.5	Transcript	5_prime_UTR_variant	119	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1121;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000514944.5	Transcript	5_prime_UTR_variant	60	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1495;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3027;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000604348.5	Transcript	5_prime_UTR_variant	120	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	114	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	114	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1121;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1121;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1121;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	117	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	171	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	114	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	124	-	-	-	-	rs1057522035	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=2/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
384728	17:7676614-7676614	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1057522035	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000269305.9	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000359597.8	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=42;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000413465.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=42;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000420246.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000445888.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000455263.6	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000503591.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1143;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1143;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000505014.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=1/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000508793.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1555527049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1143;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000514944.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1517;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3049;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000604348.5	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000610292.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000610538.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1143;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1143;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs1555527049	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1143;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000619485.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000620739.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000622645.4	Transcript	splice_polypyrimidine_tract_variant,intron_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	ENSG00000141510	ENST00000635293.1	Transcript	splice_polypyrimidine_tract_variant,intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1555527049	IMPACT=LOW;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
507871	17:7676636-7676636	C	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1555527049	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000359597.8	Transcript	upstream_gene_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=140;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000413465.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=140;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1241;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1241;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=1/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1241;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1615;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3147;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1241;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1241;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1241;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign;PHENO=1
1292419	17:7676734-7676734	T	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs8079544	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000359597.8	Transcript	upstream_gene_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=205;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000413465.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=205;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1306;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1306;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=1/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1306;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1680;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3212;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1306;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1306;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1306;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
677859	17:7676799-7676799	G	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs140699530	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000359597.8	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=345;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000413465.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=345;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=1/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1820;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3352;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1242213	17:7676938-7676939	-	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;BIOTYPE=enhancer
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000359597.8	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=345;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000413465.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=345;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=1/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1820;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3352;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1446;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998
1277877	17:7676938-7676940	-	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs34576726	IMPACT=MODIFIER;BIOTYPE=enhancer
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000359597.8	Transcript	upstream_gene_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=369;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000413465.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=369;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=2/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000504290.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1470;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000504937.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1470;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=1/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000508793.5	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000510385.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1470;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000574684.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding_CDS_not_defined;DISTANCE=1844;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000576024.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=3376;STRAND=-1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000610623.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1470;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000618944.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1470;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000619186.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1470;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
1220272	17:7676963-7676963	A	-	ENSR00000548582	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs9894227	IMPACT=MODIFIER;BIOTYPE=enhancer;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141499	ENST00000316024.9	Transcript	5_prime_UTR_variant	808	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141499	ENST00000396463.7	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=1369;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141499	ENST00000431639.6	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141499	ENST00000457584.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=332;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141499	ENST00000467699.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=retained_intron;DISTANCE=1369;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141499	ENST00000498311.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=492;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=1/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141499	ENST00000534050.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=1369;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000571370.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=737;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141499	ENST00000698742.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=805;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141499	ENST00000698743.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=1327;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141499	ENST00000698744.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=1360;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141499	ENST00000698745.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=1360;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141499	ENST00000698746.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=1370;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	ENSG00000141499	ENST00000698747.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=2534;STRAND=1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
224043	17:7687108-7687108	T	-	ENSR00000090892	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs869312655	IMPACT=MODIFIER;BIOTYPE=promoter;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000269305.9	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141499	ENST00000316024.9	Transcript	5_prime_UTR_variant	1068	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141499	ENST00000396463.7	Transcript	upstream_gene_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=1109;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CANONICAL=YES;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000420246.6	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141499	ENST00000431639.6	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000445888.6	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000455263.6	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141499	ENST00000457584.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=72;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141499	ENST00000467699.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=retained_intron;DISTANCE=1109;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141499	ENST00000498311.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=232;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000503591.1	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000505014.5	Transcript	intron_variant,non_coding_transcript_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;INTRON=1/4;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000509690.5	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000514944.5	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141499	ENST00000534050.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=1109;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000571370.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=997;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000604348.5	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/4;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000610292.4	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/9;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000610538.4	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000619485.4	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000620739.4	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000622645.4	Transcript	intron_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141510	ENST00000635293.1	Transcript	intron_variant,NMD_transcript_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;INTRON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141499	ENST00000698742.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=545;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141499	ENST00000698743.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=1067;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141499	ENST00000698744.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=1100;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141499	ENST00000698745.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=1100;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141499	ENST00000698746.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=1110;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	ENSG00000141499	ENST00000698747.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=2274;STRAND=1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	-	ENSR00000090892	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;BIOTYPE=promoter;CLIN_SIG=likely_benign;PHENO=1
516754	17:7687368-7687368	A	-	ENSM00041896088	MotifFeature	TF_binding_site_variant	-	-	-	-	-	rs1053179984	IMPACT=MODIFIER;STRAND=1;CLIN_SIG=likely_benign;PHENO=1;MOTIF_NAME=ENSPFM0134;MOTIF_POS=4;HIGH_INF_POS=Y;MOTIF_SCORE_CHANGE=-0.051;TRANSCRIPTION_FACTORS=ETV2::CEBPD,ETV2::TEF,ERF::CEBPD,ELK1::TEF,FLI1::CEBPB,FLI1::CEBPD,ETV5::CEBPD
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000269305.9	Transcript	5_prime_UTR_variant	100	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141499	ENST00000316024.9	Transcript	5_prime_UTR_variant	1091	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141499	ENST00000396463.7	Transcript	upstream_gene_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=1086;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CANONICAL=YES;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000420246.6	Transcript	5_prime_UTR_variant	91	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141499	ENST00000431639.6	Transcript	intron_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000445888.6	Transcript	5_prime_UTR_variant	97	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000455263.6	Transcript	5_prime_UTR_variant	91	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141499	ENST00000457584.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=49;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141499	ENST00000467699.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=retained_intron;DISTANCE=1086;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141499	ENST00000498311.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=209;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000503591.1	Transcript	5_prime_UTR_variant	37	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000505014.5	Transcript	non_coding_transcript_exon_variant	97	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;EXON=1/5;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000509690.5	Transcript	5_prime_UTR_variant	97	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000514944.5	Transcript	5_prime_UTR_variant	37	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/6;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141499	ENST00000534050.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=1086;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000571370.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1020;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000604348.5	Transcript	5_prime_UTR_variant	97	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/5;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000610292.4	Transcript	5_prime_UTR_variant	91	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/10;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000610538.4	Transcript	5_prime_UTR_variant	91	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000619485.4	Transcript	5_prime_UTR_variant	97	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000620739.4	Transcript	5_prime_UTR_variant	148	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/11;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000622645.4	Transcript	5_prime_UTR_variant	91	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;EXON=1/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141510	ENST00000635293.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	101	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;EXON=1/12;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141499	ENST00000698742.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=522;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141499	ENST00000698743.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=1044;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141499	ENST00000698744.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=1077;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141499	ENST00000698745.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=1077;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141499	ENST00000698746.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=1087;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	ENSG00000141499	ENST00000698747.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=2251;STRAND=1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
803312	17:7687391-7687391	A	-	ENSR00000090892	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs1166313179,COSV104370761	IMPACT=MODIFIER;BIOTYPE=promoter;CLIN_SIG=likely_benign;SOMATIC=0,1;PHENO=1,1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000269305.9	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=914;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141499	ENST00000316024.9	Transcript	5_prime_UTR_variant	2104	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141499	ENST00000396463.7	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=73;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000420246.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=923;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141499	ENST00000431639.6	Transcript	intron_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000445888.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=917;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000455263.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=923;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141499	ENST00000457584.6	Transcript	intron_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141499	ENST00000467699.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=retained_intron;DISTANCE=73;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141499	ENST00000498311.5	Transcript	5_prime_UTR_variant,NMD_transcript_variant	805	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=1/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000503591.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=977;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000505014.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=917;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000509690.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=917;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000514944.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=977;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141499	ENST00000534050.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=73;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000571370.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=2033;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000604348.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=917;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000610292.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=923;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000610538.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=923;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000619485.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=917;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000620739.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=866;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000622645.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=923;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141510	ENST00000635293.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=913;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141499	ENST00000698742.1	Transcript	5_prime_UTR_variant	492	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=1/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141499	ENST00000698743.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=31;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141499	ENST00000698744.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=64;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141499	ENST00000698745.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=64;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141499	ENST00000698746.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=74;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	ENSG00000141499	ENST00000698747.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=1238;STRAND=1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	-	ENSR00000090892	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;BIOTYPE=promoter;CLIN_SIG=benign,likely_benign;PHENO=1
369235	17:7688404-7688404	C	-	ENSM00193154578	MotifFeature	TF_binding_site_variant	-	-	-	-	-	rs17883670	IMPACT=MODIFIER;STRAND=1;CLIN_SIG=benign,likely_benign;PHENO=1;MOTIF_NAME=ENSPFM0066;MOTIF_POS=3;HIGH_INF_POS=N;MOTIF_SCORE_CHANGE=0.058;TRANSCRIPTION_FACTORS=E2F1::ELK1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000269305.9	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=953;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141499	ENST00000316024.9	Transcript	5_prime_UTR_variant	2143	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141499	ENST00000396463.7	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=34;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CANONICAL=YES;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000420246.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=962;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141499	ENST00000431639.6	Transcript	intron_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000445888.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=956;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000455263.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=962;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141499	ENST00000457584.6	Transcript	intron_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;INTRON=1/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141499	ENST00000467699.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=retained_intron;DISTANCE=34;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141499	ENST00000498311.5	Transcript	5_prime_UTR_variant,NMD_transcript_variant	844	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=1/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000503591.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1016;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000505014.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=956;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000509690.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=956;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000514944.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1016;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141499	ENST00000534050.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=34;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000571370.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=2072;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000604348.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=956;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000610292.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=962;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000610538.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=962;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000619485.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=956;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000620739.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=905;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000622645.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=962;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141510	ENST00000635293.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=952;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141499	ENST00000698742.1	Transcript	5_prime_UTR_variant	531	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=1/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141499	ENST00000698743.1	Transcript	5_prime_UTR_variant,NMD_transcript_variant	9	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=1/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141499	ENST00000698744.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=25;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141499	ENST00000698745.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=25;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141499	ENST00000698746.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=35;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	ENSG00000141499	ENST00000698747.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=1199;STRAND=1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	-	ENSR00000090892	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;BIOTYPE=promoter;CLIN_SIG=benign,likely_benign;PHENO=1
369236	17:7688443-7688443	A	-	ENSM00193455153	MotifFeature	TF_binding_site_variant	-	-	-	-	-	rs17551150	IMPACT=MODIFIER;STRAND=-1;CLIN_SIG=benign,likely_benign;PHENO=1;MOTIF_NAME=ENSPFM0070;MOTIF_POS=2;HIGH_INF_POS=N;MOTIF_SCORE_CHANGE=-0.013;TRANSCRIPTION_FACTORS=E2F1::EOMES,E2F3::EOMES,E2F3::TBX21
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000269305.9	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1752;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CANONICAL=YES;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141499	ENST00000316024.9	Transcript	synonymous_variant	2798	450	150	F	ttC/ttT	rs2287498,COSV52807243	IMPACT=LOW;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=2/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141499	ENST00000396463.7	Transcript	synonymous_variant	536	450	150	F	ttC/ttT	rs2287498,COSV52807243	IMPACT=LOW;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CANONICAL=YES;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000420246.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1761;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141499	ENST00000431639.6	Transcript	synonymous_variant	605	450	150	F	ttC/ttT	rs2287498,COSV52807243	IMPACT=LOW;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000445888.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1755;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000455263.6	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1761;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141499	ENST00000457584.6	Transcript	synonymous_variant	615	450	150	F	ttC/ttT	rs2287498,COSV52807243	IMPACT=LOW;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141499	ENST00000467699.5	Transcript	non_coding_transcript_exon_variant	536	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=retained_intron;EXON=3/9;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141499	ENST00000498311.5	Transcript	synonymous_variant,NMD_transcript_variant	1413	450	150	F	ttC/ttT	rs2287498,COSV52807243	IMPACT=LOW;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=3/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000503591.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1815;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000505014.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=1755;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000509690.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1755;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000514944.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1815;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141499	ENST00000534050.5	Transcript	intron_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;INTRON=1/8;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000571370.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=retained_intron;DISTANCE=2871;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000604348.5	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1755;STRAND=-1;FLAGS=cds_end_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000610292.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1761;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000610538.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1761;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000619485.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1755;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000620739.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1704;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000622645.4	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=protein_coding;DISTANCE=1761;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141510	ENST00000635293.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=TP53;BIOTYPE=nonsense_mediated_decay;DISTANCE=1751;STRAND=-1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:11998;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141499	ENST00000698742.1	Transcript	synonymous_variant	1100	450	150	F	ttC/ttT	rs2287498,COSV52807243	IMPACT=LOW;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=3/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141499	ENST00000698743.1	Transcript	synonymous_variant,NMD_transcript_variant	578	450	150	F	ttC/ttT	rs2287498,COSV52807243	IMPACT=LOW;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=3/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141499	ENST00000698744.1	Transcript	synonymous_variant,NMD_transcript_variant	545	450	150	F	ttC/ttT	rs2287498,COSV52807243	IMPACT=LOW;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=3/12;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141499	ENST00000698745.1	Transcript	synonymous_variant,NMD_transcript_variant	545	450	150	F	ttC/ttT	rs2287498,COSV52807243	IMPACT=LOW;SYMBOL=WRAP53;BIOTYPE=nonsense_mediated_decay;EXON=3/11;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141499	ENST00000698746.1	Transcript	synonymous_variant	535	450	150	F	ttC/ttT	rs2287498,COSV52807243	IMPACT=LOW;SYMBOL=WRAP53;BIOTYPE=protein_coding;EXON=3/10;STRAND=1;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	ENSG00000141499	ENST00000698747.1	Transcript	upstream_gene_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;SYMBOL=WRAP53;BIOTYPE=protein_coding;DISTANCE=400;STRAND=1;FLAGS=cds_start_NF;SYMBOL_SOURCE=HGNC;HGNC_ID=HGNC:25522;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1
261003	17:7689242-7689242	T	-	ENSR00000090892	RegulatoryFeature	regulatory_region_variant	-	-	-	-	-	rs2287498,COSV52807243	IMPACT=MODIFIER;BIOTYPE=promoter;CLIN_SIG=benign,likely_benign;SOMATIC=0,1;PHENO=1,1